
物理性质
- 熔点106~107 °C
- 沸点116 °C
- 闪点41 °C
- 密度1.3±0.1 g/cm3
- pKa:-0.43±0.50(预测)
- PSA:62.75
- LogP:0.93
- 折射率1.563
- 蒸汽压69.8Pa at 20°C
- 溶解性DMSO (Slightly), Methanol (Slightly)
- 敏感性1.与金属,强氧化剂,强碱,胺类,硝酸铵,三氟化氯,硝酸, 高锰酸盐,过氧化钠,过氧化氢,乙醛,酸(矿物,氧化,如铬酸,次氯酸,硝酸,硫酸) ,腐蚀剂(如氨,氢氧化铵,氢氧化钙,氢氧化钾,氢氧化钠) ,氯磺酸,发烟硫酸,溴五氟化,高氯酸,钾叔丁醇反应。 2.具有中等毒性。刺激皮肤、眼睛和黏膜。大鼠经口LD502480mg/kg,小鼠经口LD50400mg/kg。其钠盐无毒。生产过程中使用的甲苯具有毒性,对人体的肝和造血系统以及神经系统有损害。浓硫酸具有极强的腐蚀性,因此生产系统设备应保持良好的密闭性,防止泄漏,操作人员应穿戴防护用具。
- 外观形态透明无色至淡黄色溶液
- 储存条件惰性气氛,室温
- 产品应用医药上用作合成强力霉素,潘生丁,萘普生,阿莫西林,头孢羟氨苄中间体的重要原料,在有机合成工业中被广泛使用;在丙稀酸酯,纺织助剂,摄影胶片等生产中用作催化剂;在树脂,涂料,人造板,铸造,油漆行业被广泛用作固化剂,使用本厂产品,固化速度快,漆膜不变色. 本产品也是合成乙氧基喹啉的重要原料.在农药合成行业中也被广泛使用.贮运与防护:应贮存于通风干燥处,防止日晒,雨淋,露置于空气中易吸湿潮解.若吸湿后影响使用,可用离心机重新脱水或烘干.使用操作时避免与人体及衣物接触,若溅及人体或衣物应及时用水清洗.技术指标:
- 性质描述白色叶状或柱状结晶.熔点106-107°C,沸点140°C(2.67kPa).易溶于水,溶于醇和醚,难溶于苯和甲苯.该品有时以含1分子或4分子结晶水的形态存在.
欧盟法规
统一分类与标签REACH注册ECHA物质ECHA物质工作场所安全标识要求C&L通报REACH预注册废弃物危险特性清单上下游产品
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- 104-15-4 = 104-15-4
反应条件:1.1 Solvents: Methanol,Benzene
标题:Highly Active Oligomeric (Salen)Co Catalysts For Asymmetric Epoxide Ring-Opening Reactions
作者:Ready,Joseph M.; Jacobsen,Eric N.
参考文献:Journal Of The American Chemical S°Ciety 日期:2001 卷标:123(11) 页码:2687-2688]
104-15-4 = 104-15-4
反应条件:1.1 Solvents: Acetone; 30 Min,Rt
标题:Hydrogen-Bond-Assisted Organ°Catalytic Acetalization Of Secondary Alcohols: Experimental And Theoretical Studies
作者:Rumyantsev,Misha; Sitnikov,Nikolay S.; Somov,Nikolay V.
参考文献:Journal Of Physical Chemistry A 日期:2015 卷标:119(18) 页码:4108-4117]
556-02-5 + 104-15-4 + 100-51-6 = 104-15-4 + 97984-62-8
反应条件:1.1 Solvents: Benzene; 15 H,Reflux
标题:Characterization Of Spatially Addressable Libraries: Stereoisomer Analysis Of Tetrahydro-β-Carbolines As An Example
作者:Cheng,Cesar C.; Chu,Yen-Ho
参考文献:Journal Of Combinatorial Chemistry 日期:1999 卷标:1(6) 页码:461-466]
97990-19-7 + 80-48-8 = 104-15-4 + 97990-15-3
反应条件:1.1 Solvents: Acetonitrile
标题:Phot°Chemical Formation Of Methylenecyclopropane Analogs. 11. Phot°Chemical Elimination Of Nitrogen From Phenyl-Substituted 1,4-Dihydro-5-Imino-5H-Tetrazoles. Products Of Phenyl-Substituted Tris(Imino)Methane Diradicals
作者:Quast,Helmut; Fuss,Andreas; Nahr,Uwe
参考文献:Chemische Berichte 日期:1985 卷标:118(6) 页码:2164-85]
104-15-4 = 104-15-4
反应条件:1.1 Solvents: Methanol,Dichloromethane; 0 °C; 1 H,0 °C
标题:Influence Of Anion-Binding Schreiner'S Thiourea On Dmap Salts: Synergistic Catalysis Toward The Stereoselective Dehydrative Glycosylation From 2-Deoxyhemiacetals
作者:Ghosh,Titli; Mukherji,Ananya; Kancharla,Pavan K.
参考文献:Journal Of Organic Chemistry 日期:2021 卷标:86(1) 页码:1253-1261]
= 104-15-4
反应条件:1.1 Solvents: Tetrahydrofuran; Rt
标题:Synthesis,Self-Assembly,And Characterization Of Supramolecular Polymers From Electroactive Dendron Rodcoil Molecules
作者:Messmore,Benjamin W.; Hulvat,James F.; Sone,Eli D.; Stupp,Samuel I.
参考文献:Journal Of The American Chemical S°Ciety 日期:2004 卷标:126(44) 页码:14452-14458]
104-15-4 = 104-15-4
反应条件:1.1 Solvents: Ethyl Acetate; 4 H; Overnight,Cooled
标题:Integration Of Upcycling And Closed-Loop Recycling Through Alternative Cyclization-Depolymerization
作者:Tian,Guo-Qiang; Yang,Zheng-He; Zhang,Wei; Chen,Si-Chong; Chen,Li; Et Al
参考文献:Green Chemistry 日期:2022 卷标:24(11) 页码:4490-4497]
104-15-4 = 104-15-4
反应条件:1.1 Solvents: Benzene; Heated
标题:Chiral Compounds With Liquid Crystalline Nature And Ferroelectric Liquid Crystal Device Adopting The Same
参考文献:World Intellectual Property Organization]
= 104-15-4
反应条件:1.1 Solvents: Tetrahydrofuran; Heated
标题:Copper-Mediated Radiofluorination Of Aryl Pinacolboronate Esters: A Straightforward Prot°Col By Using Pyridinium Sulfonates
作者:Antuganov,Dmitrii; Zykov,Michail; Timofeev,Vasilii; Timofeeva,Ksenija; Antuganova,Yulija; Et Al
参考文献:European Journal Of Organic Chemistry 日期:2019 卷标:2019(5) 页码:918-922]
= 104-15-4
反应条件:1.1 Solvents: Tetrahydrofuran; 30 Min,Rt
标题:Fluorescent Macromolecular Perylene Diimides Containing Pyrene Or Indole Units In Bay Positions
作者:Dincalp,Haluk; Kizilok,Sevki; Icli,Siddik
参考文献:Dyes And Pigments 日期:2010 卷标:86(1) 页码:32-41]
104-15-4 = 104-15-4
反应条件:1.1 Solvents: Toluene; 1 H,60 °C
标题:Degradable Amino Acid-Based Poly(Ester Urea) Copolymer Adhesives
参考文献:World Intellectual Property Organization]
104-15-4 = 104-15-4
反应条件:1.1 Solvents: Toluene; 24 H,Reflux
标题:A Quantitative Assessment Of Chemical Perturbations In Thermotropic Cyanobiphenyls
作者:Guerra,Sebastiano; Dutronc,Thibault; Terazzi,Emmanuel; Guenee,Laure; Piguet,Claude
参考文献:Physical Chemistry Chemical Physics 日期:2016 卷标:18(21) 页码:14479-14494]
104-15-4 = 104-15-4
反应条件:1.1 Solvents: Tetrahydrofuran; Rt; 10 Min,Rt
标题:Manufacture Of Gel-Like Thin Films And Composite Membranes For Gas Separation
参考文献:Japan]
104-15-4 = 104-15-4
反应条件:1.1 Solvents: Tetrahydrofuran; Rt
标题:Monodisperse Cyclic Polymer Mechan°Chemistry: Scission Kinetics And The Dynamic Memory Effect With Ultrasonication And Ball-Mill Grinding
作者:Noh,Jinkyung; Koo,Mo Beom; Jung,Jisoo; Peterson,Gregory I.; Kim,Kyoung Taek; Et Al
参考文献:Journal Of The American Chemical S°Ciety 日期:2023 卷标:145(33) 页码:18432-18438]
104-15-4 = 104-15-4 [标题:Reaction Conditions
标题:Method For The Synthesis Of Polyethers
参考文献:World Intellectual Property Organization]
= 104-15-4
反应条件:1.1 Solvents: Benzene
标题:Multifunctional Zwitterionic Polymer Conjugates For Therapeutic Use
参考文献:United States]
104-15-4 = 104-15-4 [标题:Reaction Conditions
标题:Brush-Like Poly(Ethylene Glycol) Grafting On Sio2 Nanoparticles With In-Situ Polymerization
作者:Zhao,Yanhua; Chai,Changsheng
参考文献:Surface And Interface Analysis 日期:2015 卷标:47(3) 页码:384-389]
104-15-4 + 80875-98-5 + 100-51-6 = 104-15-4
反应条件:1.1 Solvents: Toluene; 100 - 118 °C
标题:Preparation Of Novel Crystalline η (Eta) Form Of Perindopril Erbumine
参考文献:World Intellectual Property Organization]
104-15-4 + 539820-41-2 = 104-15-4
反应条件:1.1 Solvents: Acetic Acid; Rt1.2 Catalysts: Platinum; Rt1.3 Reagents: Hydrogen; 5 Bar,Rt1.4 Solvents: Toluene; Reflux
标题:Method For Synthesis Of (2S,3As,7As)-Perhydroindole-2-Carboxylic Acid And Esters As Intermediates In The Synthesis Of Perindopril
参考文献:European Patent Organization]
= 104-15-4 [标题:Reaction Conditions
标题:Pharmaceutical Intermediate For Synthesizing Ace Inhibitors And The Use Thereof
参考文献:United States]
= 104-15-4 [标题:Reaction Conditions
标题:Preparation Of Amino Acid-Derived Intermediates In The Synthesis Of Ace Inhibitors
参考文献:World Intellectual Property Organization]
= 104-15-4 [标题:Reaction Conditions
标题:Facile Synthesis Of Amino Acid Methyl Ester P-Toluenesulfonates With Methyl P-Toluenesulfonate
作者:Ueda,Kazuo; Waki,Michinori; Izumiya,Nobuo
参考文献:Memoirs Of The Faculty Of Science 日期:1984 卷标:14(2) 页码:307-12]
= 104-15-4 [标题:Reaction Conditions
标题:Synthesis,Structural,Spectroscopic,Mechanical,Linear And Nonlinear Optical Studies On 4-Dimethylaminopyridinium P-Toluenesulfonate: A Comparative Theoretical And Experimental Investigation
作者:Sivaraj,G.; Et Al
参考文献:Journal Of Molecular Structure 日期:2021 卷标:1240]
= 104-15-4 [标题:Reaction Conditions
标题:Synthesis And Characterization Of Versatile Amphiphilic Dendrimers Peripherally Decorated With Positively Charged Amino Acids
作者:Alfei,Silvana; Et Al
参考文献:Polymer International 日期:2018 卷标:67(11) 页码:1572-1584]
= 104-15-4 [标题:Reaction Conditions
标题:Corrigendum To "Sustained L°Calized Presentation Of Rna Interfering Molecules From In Situ Forming Hydrogels To Guide Stem Cell Osteogenic Differentiation" [biomaterials 35/24 (2014) 6278-6286] [erratum To D°Cument Cited In Ca161:090975]
作者:Nguyen,Minh K.; Et Al
参考文献:Biomaterials 日期:2017 卷标:125]
= 104-15-4 + 88-20-0
反应条件:1.1 Reagents: 2,4,6-Trimethylbenzenesulfonic Acid Solvents: Mesitylene
标题:Sulfonating Agent And Pr°Cess
参考文献:World Intellectual Property Organization]
615-37-2 = 104-15-4 + 103675-61-2 + 88-20-0 + 103675-62-3
反应条件:1.1 Reagents: Sulfuric Acid
标题:Studies On The Sulfonation Of O-Iodotoluene
作者:Muramoto,Yoshihiro; Et Al
参考文献:Kinki Daigaku Kogakubu Kenkyu Hokoku 日期:1985 卷标:19 页码:27-32]
72-18-4 = 104-15-4
反应条件:1.1 Solvents: Benzene; Reflux
标题:Using Peptidic Inhibitors To Systematically Probe The S1' Site Of Caspase-3 And Caspase-7
作者:Goode,David R.; Et Al
参考文献:Organic Letters 日期:2005 卷标:7(16) 页码:3529-3532]
104-15-4 + 72-18-4 = 104-15-4
反应条件:1.1 Solvents: Toluene; 24 H,Reflux
标题:Design,Synthesis,And Evaluation Of Cystargolide-Based β-Lactones As Potent Proteasome Inhibitors
作者:Niroula,Doleshwar; Et Al
参考文献:European Journal Of Medicinal Chemistry 日期:2018 卷标:157 页码:962-977]
104-15-4 = 104-15-4 + 45012-62-2
反应条件:1.1 Solvents: Toluene; Reflux
标题:Microwave-Enhanced Copper-Catalyzed N-Arylation Of Free And Protected Amino Acids In Water
作者:Roettger,Svenja; Et Al
参考文献:Journal Of Combinatorial Chemistry 日期:2007 卷标:9(2) 页码:204-209]
= 104-15-4
反应条件:1.1 Solvents: Methanol; 0.25 H,25 - 35 °C; 2 H,50 °C1.2 Reagents: Acetic Acid Solvents: Methanol; Ph 7.3,5 °C2.1 Solvents: Methanol; 20 Min,Rt; 4 H,40 °C; Overnight,Rt
标题:Synthesis Of (1R,2S)-1-Amino-2-Vinylcyclopropanecarboxylic Acid Vinyl-Acca) Derivatives: Key Intermediates For The Preparation Of Inhibitors Of The Hepatitis C Virus Ns3 Protease
作者:Beaulieu,Pierre L.; Et Al
参考文献:Journal Of Organic Chemistry 日期:2005 卷标:70(15) 页码:5869-5879]
259214-57-8 = 104-15-4
反应条件:1.1 Reagents: Sodium Hydroxide,Potassium Chloride Catalysts: Subtilisin Solvents: Acetone,Water; 91 H,Ph 8.1 - 8.3,35 - 37 °C1.2 Reagents: Hydr°Chloric Acid Solvents: Water; 75 H,Ph 2 - 3,Rt2.1 Solvents: Methanol; 20 Min,Rt; 4 H,40 °C; Overnight,Rt
标题:Synthesis Of (1R,2S)-1-Amino-2-Vinylcyclopropanecarboxylic Acid Vinyl-Acca) Derivatives: Key Intermediates For The Preparation Of Inhibitors Of The Hepatitis C Virus Ns3 Protease
作者:Beaulieu,Pierre L.; Et Al
参考文献:Journal Of Organic Chemistry 日期:2005 卷标:70(15) 页码:5869-5879]
213316-49-5 = 104-15-4
反应条件:1.1 Solvents: Methanol; 50 °C2.1 Reagents: Sodium Hydroxide,Potassium Chloride Catalysts: Subtilisin Solvents: Acetone,Water; 91 H,Ph 8.1 - 8.3,35 - 37 °C2.2 Reagents: Hydr°Chloric Acid Solvents: Water; 75 H,Ph 2 - 3,Rt3.1 Solvents: Methanol; 20 Min,Rt; 4 H,40 °C; Overnight,Rt
标题:Synthesis Of (1R,2S)-1-Amino-2-Vinylcyclopropanecarboxylic Acid Vinyl-Acca) Derivatives: Key Intermediates For The Preparation Of Inhibitors Of The Hepatitis C Virus Ns3 Protease
作者:Beaulieu,Pierre L.; Et Al
参考文献:Journal Of Organic Chemistry 日期:2005 卷标:70(15) 页码:5869-5879]
213316-49-5 = 104-15-4
反应条件:1.1 Reagents: Sodium Hydroxide,Potassium Chloride Catalysts: Subtilisin Solvents: Acetone,Water; 91 H,Ph 8.1 - 8.3,35 - 37 °C1.2 Reagents: Hydr°Chloric Acid Solvents: Water; 75 H,Ph 2 - 3,Rt2.1 Solvents: Methanol; 0.25 H,25 - 35 °C; 2 H,50 °C2.2 Reagents: Acetic Acid Solvents: Methanol; Ph 7.3,5 °C3.1 Solvents: Methanol; 20 Min,Rt; 4 H,40 °C; Overnight,Rt
标题:Synthesis Of (1R,2S)-1-Amino-2-Vinylcyclopropanecarboxylic Acid Vinyl-Acca) Derivatives: Key Intermediates For The Preparation Of Inhibitors Of The Hepatitis C Virus Ns3 Protease
作者:Beaulieu,Pierre L.; Et Al
参考文献:Journal Of Organic Chemistry 日期:2005 卷标:70(15) 页码:5869-5879]
24424-99-5 = 104-15-4
反应条件:1.1 Reagents: Sodium Hydroxide Solvents: Tetrahydrofuran,Water; 0.75 H,24 °C; 22 H,20 °C2.1 Solvents: Methanol; 0.25 H,25 - 35 °C; 2 H,50 °C2.2 Reagents: Acetic Acid Solvents: Methanol; Ph 7.3,5 °C3.1 Solvents: Methanol; 20 Min,Rt; 4 H,40 °C; Overnight,Rt
标题:Synthesis Of (1R,2S)-1-Amino-2-Vinylcyclopropanecarboxylic Acid Vinyl-Acca) Derivatives: Key Intermediates For The Preparation Of Inhibitors Of The Hepatitis C Virus Ns3 Protease
作者:Beaulieu,Pierre L.; Et Al
参考文献:Journal Of Organic Chemistry 日期:2005 卷标:70(15) 页码:5869-5879]
24424-99-5 = 104-15-4
反应条件:1.1 Reagents: Lithium Tert-Butoxide Solvents: Toluene1.2 Reagents: Hydr°Chloric Acid Solvents: Water; 2 H,Rt1.3 Reagents: Sodium Hydroxide Solvents: Tert-Butyl Methyl Ether,Water; Ph 12 - 131.4 Overnight,Rt; 2 H,60 °C2.1 Reagents: Sodium Hydroxide,Potassium Chloride Catalysts: Subtilisin Solvents: Acetone,Water; 91 H,Ph 8.1 - 8.3,35 - 37 °C2.2 Reagents: Hydr°Chloric Acid Solvents: Water; 75 H,Ph 2 - 3,Rt3.1 Solvents: Methanol; 0.25 H,25 - 35 °C; 2 H,50 °C3.2 Reagents: Acetic Acid Solvents: Methanol; Ph 7.3,5 °C4.1 Solvents: Methanol; 20 Min,Rt; 4 H,40 °C; Overnight,Rt
标题:Synthesis Of (1R,2S)-1-Amino-2-Vinylcyclopropanecarboxylic Acid Vinyl-Acca) Derivatives: Key Intermediates For The Preparation Of Inhibitors Of The Hepatitis C Virus Ns3 Protease
作者:Beaulieu,Pierre L.; Et Al
参考文献:Journal Of Organic Chemistry 日期:2005 卷标:70(15) 页码:5869-5879]
623-33-6 = 104-15-4
反应条件:1.1 Reagents: Triethylamine,Sodium Sulfate Solvents: Tert-Butyl Methyl Ether; 0.17 H,5 °C; 24 H,Rt2.1 Reagents: Lithium Tert-Butoxide Solvents: Toluene2.2 Reagents: Hydr°Chloric Acid Solvents: Water; 2 H,Rt2.3 Reagents: Sodium Hydroxide Solvents: Tert-Butyl Methyl Ether,Water; Ph 12 - 132.4 Overnight,Rt; 2 H,60 °C3.1 Reagents: Sodium Hydroxide,Potassium Chloride Catalysts: Subtilisin Solvents: Acetone,Water; 91 H,Ph 8.1 - 8.3,35 - 37 °C3.2 Reagents: Hydr°Chloric Acid Solvents: Water; 75 H,Ph 2 - 3,Rt4.1 Solvents: Methanol; 0.25 H,25 - 35 °C; 2 H,50 °C4.2 Reagents: Acetic Acid Solvents: Methanol; Ph 7.3,5 °C5.1 Solvents: Methanol; 20 Min,Rt; 4 H,40 °C; Overnight,Rt
标题:Synthesis Of (1R,2S)-1-Amino-2-Vinylcyclopropanecarboxylic Acid Vinyl-Acca) Derivatives: Key Intermediates For The Preparation Of Inhibitors Of The Hepatitis C Virus Ns3 Protease
作者:Beaulieu,Pierre L.; Et Al
参考文献:Journal Of Organic Chemistry 日期:2005 卷标:70(15) 页码:5869-5879]
= 104-15-4 + 97984-62-8 [标题:Reaction Conditions
标题:Synthesis Of Analogs Of K-582A,An Antibiotic Heptapeptide
作者:Mihara,Hisakazu; Aoyagi,Haruhiko; Yonezawa,Hiroo; Kuromizu,Kenji; Izumiya,Nobuo
参考文献:International Journal Of Peptide & Protein Research 日期:1985 卷标:25(6) 页码:640-7]
= 104-15-4
反应条件:1.1 Solvents: Acetonitrile,Tetrahydrofuran; 2 H,50 - 60 °C; 50 °C -> Reflux; 70 - 80 °C
标题:Treatment Of Cystic Fibrosis Or The Symptoms Ass°Ciatedd With Cystic Fibrosis
参考文献:United States]
104-15-4 = 104-15-4
反应条件:1.1 Solvents: Acetonitrile,Tetrahydrofuran; Rt -> 37 °C; 33 - 37 °C
标题:Preparation Of N-[4-Chloro-2-Hydroxy-3-(Piperazine-1-Sulfonyl)Phenyl]-N'-(2-Chloro-3-Fluorophenyl)Urea For Treatment Of Cystic Fibrosis
参考文献:World Intellectual Property Organization]
= 104-15-4 [标题:Reaction Conditions
标题:Il-8 Receptor Antagonist
参考文献:World Intellectual Property Organization]
104-15-4 + 80875-98-5 = 104-15-4
反应条件:1.1 Solvents: Toluene; Rt -> 110 °C; 14 H,110 °C
标题:Preparation Of Perindopril Tert-Butylamine Salt
参考文献:China]
104-15-4 + 80875-98-5 + 100-51-6 = 104-15-4
反应条件:1.1 Catalysts: P-Toluenesulfonic Acid Solvents: Toluene
标题:Method For Synthesis Of (2S,3As,7As)-Perhydroindole-2-Carboxylic Acid And Esters As Intermediates In The Synthesis Of Perindopril
参考文献:European Patent Organization]
104-15-4 + 80875-98-5 + 100-51-6 = 104-15-4
反应条件:1.1 Solvents: Toluene; 100 - 118 °C
标题:Preparation Of Novel Crystalline Form Of Perindopril Erbumine Monohydrate
参考文献:World Intellectual Property Organization]
= 104-15-4 [标题:Reaction Conditions
标题:Configuration And Preferential Solid-State Conformations Of Perindoprilat (S-9780). Comparison With The Crystal Structures Of Other Ace Inhibitors And Conclusions Related To Structure-Activity Relationships
作者:Pascard,Claudine; Guilhem,Jean; Vincent,Michel; Remond,Georges; Portevin,Bernard; Et Al
参考文献:Journal Of Medicinal Chemistry 日期:1991 卷标:34(2) 页码:663-9]
= 104-15-4 [标题:Reaction Conditions
标题:Preparation Of Perindopril Via Acylation Of Perhydroindolecarboxylate With N-[(Ethoxycarbonyl)Butyl]Alanine
参考文献:European Patent Organization]
= 104-15-4 [标题:Reaction Conditions
标题:Racemate Separation Of Optically Active Bicyclic Imino-α-Carboxylic Acids
参考文献:Federal Republic Of Germany]
104-15-4 = 104-15-4
反应条件:1.1 Solvents: Tetrahydrofuran; Rt
标题:A Hydrophilic Coumarin-Based Polyester For Ambient-Temperature Initiator-Free 3D Printing: Chemistry,Rheology And Interface Formation
作者:Govindarajan,Sudhanva R.; Jain,Tanmay; Choi,Jae-Won; Joy,Abraham; Isayeva,Irada; Et Al
参考文献:Polymer 日期:2018 卷标:152 页码:9-17]
= 104-15-4
反应条件:1.1 Solvents: Toluene; 60 °C; 1 H,60 °C
标题:Co-Initiated Hyperbranched-Polydendron Building Bl°Cks For The Direct Nanoprecipitation Of Dendron-Directed Patchy Particles With Heterogeneous Surface Functionality
作者:Hern,F. Y.; Hill,A.; Owen,A.; Rannard,S. P.
参考文献:Polymer Chemistry 日期:2018 卷标:9(14) 页码:1767-1771]
104-15-4 = 104-15-4
反应条件:1.1 Solvents: Toluene; 1 H,60 °C
标题:Adhesion Properties Of Catechol-Based Biodegradable Amino Acid-Based Poly(Ester Urea) Copolymers Inspired From Mussel Proteins
作者:Zhou,Jinjun; Defante,Adrian P.; Lin,Fei; Xu,Ying; Yu,Jiayi; Et Al
参考文献:Biomacromolecules 日期:2015 卷标:16(1) 页码:266-274]
104-15-4 = 104-15-4 [标题:Reaction Conditions
标题:Multifunctional Polymer Nan°Carrier For Efficient Targeted Cellular And Subcellular Anticancer Drug Delivery
作者:Babikova,Dimitrina; Kalinova,Radostina; Momekova,Denitsa; Ugrinova,Iva; Momekov,Georgi; Et Al
参考文献:Acs Biomaterials Science & Engineering 日期:2019 卷标:5(5) 页码:2271-2283]
104-15-4 = 104-15-4 [标题:Reaction Conditions
标题:Reversible Phot°Curing Of Liquid Hexa-Anthracene Compounds For Adhesive Applications
作者:Akiyama,Haruhisa; Okuyama,Yoko; Fukata,Tamaki; Kihara,Hideyuki
参考文献:Journal Of Adhesion 日期:2018 卷标:94(10) 页码:799-813]
104-15-4 = 104-15-4
反应条件:1.1 Solvents: Toluene; Heated1.2 Solvents: Toluene; Heated; Rt
标题:Uv-Cured Hyperbranched Polyester Polythiol(H20-Sh)-Epoxy Acrylate Networks: Preparation,Thermal And Mechanical Properties
作者:Guan,Xiao-Xiao; Gan,Jian-Qun; Chen,Guo-Kang; Huang,Xiao-Mei; Lu,Man-Geng; Et Al
参考文献:Journal Of Macromolecular Science 日期:2017 卷标:54(10) 页码:662-668]
= 104-15-4
反应条件:1.1 Solvents: Tetrahydrofuran; 1 H,Rt
标题:Synthesis And Phot°Chemical Properties Of 3,6-Di-Tert-Butyl-9H-Carbazole Derivatives
作者:Gruzdev,M. S.; Chervonova,U. V.; Venediktov,E. A.; Rozhkova,E. P.; Kolker,A. M.; Et Al
参考文献:Russian Journal Of General Chemistry 日期:2015 卷标:85(6) 页码:1431-1439]
= 104-15-4 + 88-20-0
反应条件:1.1 Reagents: Sulfuric Acid (Silica Supported); 30 Min,80 °C
标题:A Novel Method For Sulfonation Of Aromatic Rings With Silica Sulfuric Acid
作者:Hajipour,Abdol R.; Et Al
参考文献:Tetrahedron Letters 日期:2004 卷标:45(35) 页码:6607-6609]
= 104-15-4 + 88-20-0
反应条件:1.1 Reagents: Sulfur Trioxide; 58.5 °C
标题:Study On The Sulfonation Of Toluene With So3 In Microreactor
作者:Chen,Yanquan; Et Al
参考文献:Huaxue Fanying Gongcheng Yu Gongyi 日期:2013 卷标:29(3) 页码:253-259]
104-15-4 = 104-15-4 + 429658-95-7
反应条件:1.1 Reagents: Hydr°Chloric Acid Solvents: Ethanol1.2 Reagents: Ammonium Hydroxide Solvents: Water
标题:Identification,Synthesis,And Strategy For The Reduction Of Potential Impurities Observed In Dabigatran Etexilate Mesylate Pr°Cesses
作者:Zheng,Yong-Yong; Et Al
参考文献:Organic Pr°Cess Research & Development 日期:2014 卷标:18(6) 页码:744-750]
= 104-15-4
反应条件:1.1 Solvents: Methanol; 20 Min,Rt; 4 H,40 °C; Overnight,Rt
标题:Synthesis Of (1R,2S)-1-Amino-2-Vinylcyclopropanecarboxylic Acid Vinyl-Acca) Derivatives: Key Intermediates For The Preparation Of Inhibitors Of The Hepatitis C Virus Ns3 Protease
作者:Beaulieu,Pierre L.; Et Al
参考文献:Journal Of Organic Chemistry 日期:2005 卷标:70(15) 页码:5869-5879]
24424-99-5 = 104-15-4
反应条件:1.1 Reagents: Lithium Tert-Butoxide Solvents: Toluene1.2 Reagents: Hydr°Chloric Acid Solvents: Water; 2 H,Rt1.3 Reagents: Sodium Hydroxide Solvents: Tert-Butyl Methyl Ether,Water; Ph 12 - 131.4 Overnight,Rt; 2 H,60 °C2.1 Reagents: Sodium Hydroxide,Potassium Chloride Catalysts: Subtilisin Solvents: Acetone,Water; 91 H,Ph 8.1 - 8.3,35 - 37 °C2.2 Reagents: Hydr°Chloric Acid Solvents: Water; 75 H,Ph 2 - 3,Rt3.1 Solvents: Methanol; 20 Min,Rt; 4 H,40 °C; Overnight,Rt
标题:Synthesis Of (1R,2S)-1-Amino-2-Vinylcyclopropanecarboxylic Acid Vinyl-Acca) Derivatives: Key Intermediates For The Preparation Of Inhibitors Of The Hepatitis C Virus Ns3 Protease
作者:Beaulieu,Pierre L.; Et Al
参考文献:Journal Of Organic Chemistry 日期:2005 卷标:70(15) 页码:5869-5879]
= 104-15-4
反应条件:1.1 Solvents: Ethanol; 2 H,60 °C; 6 H,60 °C -> 25 °C; 18 H,Rt2.1 Reagents: Sodium Hydroxide Solvents: Tetrahydrofuran,Water; 0.75 H,24 °C; 22 H,20 °C3.1 Solvents: Methanol; 0.25 H,25 - 35 °C; 2 H,50 °C3.2 Reagents: Acetic Acid Solvents: Methanol; Ph 7.3,5 °C4.1 Solvents: Methanol; 20 Min,Rt; 4 H,40 °C; Overnight,Rt
标题:Synthesis Of (1R,2S)-1-Amino-2-Vinylcyclopropanecarboxylic Acid Vinyl-Acca) Derivatives: Key Intermediates For The Preparation Of Inhibitors Of The Hepatitis C Virus Ns3 Protease
作者:Beaulieu,Pierre L.; Et Al
参考文献:Journal Of Organic Chemistry 日期:2005 卷标:70(15) 页码:5869-5879]
= 104-15-4
反应条件:1.1 Reagents: Lithium Tert-Butoxide Solvents: Toluene1.2 Reagents: Hydr°Chloric Acid Solvents: Water; 2 H,Rt1.3 Reagents: Sodium Hydroxide Solvents: Water2.1 Solvents: Ethanol; 2 H,60 °C; 6 H,60 °C -> 25 °C; 18 H,Rt3.1 Reagents: Sodium Hydroxide Solvents: Tetrahydrofuran,Water; 0.75 H,24 °C; 22 H,20 °C4.1 Solvents: Methanol; 0.25 H,25 - 35 °C; 2 H,50 °C4.2 Reagents: Acetic Acid Solvents: Methanol; Ph 7.3,5 °C5.1 Solvents: Methanol; 20 Min,Rt; 4 H,40 °C; Overnight,Rt
标题:Synthesis Of (1R,2S)-1-Amino-2-Vinylcyclopropanecarboxylic Acid Vinyl-Acca) Derivatives: Key Intermediates For The Preparation Of Inhibitors Of The Hepatitis C Virus Ns3 Protease
作者:Beaulieu,Pierre L.; Et Al
参考文献:Journal Of Organic Chemistry 日期:2005 卷标:70(15) 页码:5869-5879
对甲苯磺酸甲酯置于邻苯二甲酸二甲酯,水体系中,化学反应 3.0H,反应生成对甲苯磺酸
参考文献:Removal Of Alkyl Alkanesulfonate Esters From Alkanesulfonic Acids And Other Organic Media
标题:Removal Of Alkyl Alkanesulfonate Esters From Alkanesulfonic Acids And Other Organic Media
摘要:提供了从水性或无水性组合物中去除烷基烷磺酸酯的方法.该发明提供了将化学式为rso3R'的烷基烷磺酸酯转化为化学式为rso3H的相应酸的方法.烷基烷磺酸酯存在于有机介质中,该介质可能含有大量水,也可能是无水或基本无水的.在某些实施例中,该发明提供了通过去除烷基烷磺酸酯来净化水性或无水烷磺酸的方法.
专利信息
专利号:US-6504041-B2
优先权日:1996-11-15
标题 :Synthesis of ruthenium or osmium metathesis catalysts
发明人:GRUBBS ROBERT H; BELDERRAIN TOMAS R; BROWN SETH N; WILHELM THOMAS E
权利人:CALIFORNIA INST OF TECHN
摘要:The present invention relates to the synthesis of highly active ruthenium and osmium carbene metathesis catalyst in good yield from readily available starting materials. The catalysts that may be synthesized are of the general formula n wherein: n M is ruthenium or osmium; n X and X 1 are independently any anionic ligand; n L and L 1 are any neutral electron donor ligand; and, n R and R 1 are each hydrogen or one of the following substituent groups: C 2 -C 20 alkenyl, C 2 -C 20 alkynyl, C 1 -C 20 alkyl, aryl, C 1 -C 20 carboxylate, C 1 -C 20 alkoxy, C 2 -C 20 alkenyloxy, C 2 -C 20 alkynyloxy, aryloxy, C 2 -C 20 alkoxycarbonyl, C 1 -C 20 alkylthio, C 1 -C 20 alkylsulfonyl and C 1 -C 20 alkylsulfinyl. Optionally, the substituent group may be substituted with one or more groups selected from C 1 -C 5 alkyl, halogen, C 1 -C 5 alkoxy, and aryl. When the substitute aryl group is phenyl, it may be further substituted with one or more groups selected from a halogen, a C 1 -C 5 alkyl, or a C 1 -C 5 alkoxy. Specific synthetic protocols for vinyl alkylidene catalysts wherein R is hydrogen and R 1 is —CHCR 12 R 13 and non-vinyl alkylidene catalysts are also disclosed. In addition to the ease of synthesis (typically a one-step synthesis), the reactions generally may be run at or above room temperature and the resulting products usually may be used without extensive post synthesis purification.
专利号:US-12441721-B2
优先权日:2020-07-21
标 题 :Synthesis of heterocyclic compounds from carboxamide and carboxamide derivatives with haloalkanols
发明人:KARPOORMATH RAJSHEKHAR; SAYYAD NISAR
权利人:UNIV OF KWAZULU NATAL
摘要:The invention provides for methods for the synthesis of various compounds through reaction of carboxamide, or carboxamide derivatives, with various substituted or unsubstituted haloalkanols in a one-step, single vessel, reaction mechanism. Preferably, but not exclusively, the reaction proceeds in the absence of any solvents, catalyst, base, or any further reagents.
专利号:US-3872168-A
优先权日:1972-10-02
标题:Synthesis of acids and amides
发明人:COLLMAN JAMES P; WINTER STANLEY R; KOMOTO ROBERT G
权利人:TRUSTEES OF THE LELAND STAMFOR
摘要:Synthesis of acids R1COOH and amides R1CONR2R3 wherein R1 is attached to the carbonyl group by an aliphatic carbon atom and R2 and R3 are hydrogen or organic groups of a primary or secondary amine, by forming an alkyl or acyl intermediate (R1Fe(CO) 4 or R1COFe(CO) 4) and treating the intermediate with a suitable cleaving agent and, in the case of amides, also with ammonia or an amine.
专利号:EP-4092127-A1
优先权日:2021-05-18
标题:Enzyme-catalytic method for the direct stereoselective synthesis of gamma-(acyloxy) carboxylic acids
发明人:PARVE JAAN; KUDRJASHOVA MARINA; GATHERGOOD NICHOLAS; PARVE OMAR
权利人:TALLINN UNIV OF TECHNOLOGY
摘要:The present invention is a method for the stereoselective straightforward synthesis of gamma-acyloxy carboxylic acids of novel structure starting from racemic gamma-hydroxy carboxylic acid salts that are obtained by alkaline hydrolysis of the racemic gamma-lactones. The salt is acylated by enzyme catalysis in an organic solvent containing an acyl donor and an immobilised lipase, on stirring at room temperature (ca 20 °C) until reaching the conversion rate required. After that, the reaction mixture is acidified and extracted and the product treated with catalytic amount of para-toluenesulfonic acid in toluene during the time required for the relactonisation of the unreacted salt enantiomer. Thereafter, the target gamma-acyloxy carboxylic acid formed from one enantiomer of the starting compound and relactonised gamma-lactone formed from the other, unreacted enantiomer of the starting compound are isolated using a routine separation method, such as distillation, extraction with NaHCO3 water solution followed by acidification or column chromatography.
专利号:US-6794534-B2
优先权日:2000-06-23
标题:Synthesis of functionalized and unfunctionalized olefins via cross and ring-closing metathesis
发明人:GRUBBS ROBERT H; CHATTERJEE ARNAB K; MORGAN JOHN P; SCHOLL MATTHIAS; CHOI TAE-LIM
权利人:CALIFORNIA INST OF TECHN
摘要:The invention is directed to the cross-metathesis and ring-closing metathesis reactions between geminal disubstituted olefins and terminal olefins, wherein the reaction employs a Ruthenium or Osmium metal carbene complex. Specifically, the invention relates to the synthesis of α-functionalized or unfunctionalized olefins via intermolecular cross-metathesis and intramolecular ring-closing metathesis using a ruthenium alkylidene complex. The catalysts preferably used in the invention are of the general formula n wherein: n M is ruthenium or osmium; n X and X 1 are each independently an anionic ligand; n L is a neutral electron donor ligand; and, n R, R 1 R 6 , R 7 , R 8 , and R 9 are each independently hydrogen or a substituent selected from the group consisting of C 1 -C 20 alkyl, C 2 -C 20 alkenyl, C 2 -C 20 alkynyl, aryl, C 1 -C 20 carboxylate, C 1 -C 20 alkoxy, C 2 -C 20 alkenyloxy, C 2 -C 20 alkynyloxy, aryloxy, C 2 -C 20 alkoxycarbonyl, C 1 -C 20 alkylthio, C 1 -C 20 alkylsulfonyl and C 1 -C 20 alkylsulfinyl.
专利号:WO-2013138200-A1
优先权日:2012-03-13
标 题 :Green chemistry synthesis of the malaria drug amodiaquine and analogs thereof
发明人:FORTUNAK JOSEPH MARIAN; KULKARNI AMOL ANANT; KING CHRISTOPHER
权利人:UNIV HOWARD
摘要:Methods are provided for a green chemistry one-pot synthesis of amodiaquine and amodiaquine analogs. The methods have a lower environmental impact, lower investment cost, reduced amounts of byproducts and impurities, and a shorter synthesis time, compared to current conventional synthesis methods. The methods reduce the total number of steps in the synthesis from four to five down to two, thereby simplifying production; and allow a reduced number of solvents and reagents to be used in production, thereby reducing the waste generated in the synthesis. The methods can reduce the waste to about 3-5 kilograms of waste generated per kilogram of product produced; and surprisingly improve the overall yield from 60-65% to greater than 90% as compared to the current conventional synthesis methods for amodiaquine and its analogs.