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CAS号5466-84-2 4-硝基邻苯二甲酸酐 | CAS号105969-98-0 4-硝基邻苯二甲酰亚胺 | CAS号610-27-5 4-硝基邻苯二甲酸 | CAS号2516-96-3 2-氯-5-硝基苯甲酸 | CAS号85-44-9 苯酐 | CAS号46053-72-9 5-硝基异吲哚啉 | CAS号13138-53-9 4-硝基邻苯二甲酰胺 | CAS号3816-62-4 2-氨基-5-硝基苯甲酸甲酯 | CAS号3558-13-2 Methyl 2-(Methy... | CAS号3558-19-8 2-氨基-4-硝基苯甲酸甲酯 | CAS号3676-85-5 4-氨基邻苯二甲酰亚胺 | CAS号140715-56-6 2-(3-溴丙基)-5-硝基异... | CAS号140715-57-7 2-(6-溴己基)-5-硝基异... | CAS号40392-27-6 4-硝基-N-苯基邻苯二甲酰亚胺 | CAS号41663-84-7 N-甲基-4-硝基邻苯二甲酰亚胺 | CAS号3682-19-7 4-硝基邻苯二甲酰肼 | CAS号64169-34-2 5-溴苯酞合成工艺路线路线简述
- 5466-84-2 = 89-40-7
反应条件:1.1 Reagents: Ammonium Chloride Catalysts: 4-(Dimethylamino)Pyridine; 47 S
标题:Microwave-Assisted Efficient Conversion Of Anhydrides To Cyclic Imides And N-Methoxy Imides
作者:Hijji,Yousef M.; Benjamin,Ellis
参考文献:International Electronic Conferences On Synthetic Organic Chemistry 日期:2004 卷标:1084 页码:1084-1091]
5466-84-2 = 89-40-7
反应条件:1.1 Reagents: Formamide Solvents: N-Methyl-2-Pyrrolidone; Rt -> 180 °C; 5 - 6 H,170 - 180 °C
标题:Formamide,A Novel Challenging Reagent For The Direct Synthesis Of Non-N-Substituted Cyclic Imides
作者:Chiriac,Constantin I.; Nechifor,Marioara; Tanasa,Fulga
参考文献:Revue Roumaine De Chimie 日期:2007 卷标:52(8-9) 页码:883-886]
= 89-40-7
反应条件:1.1 Reagents: Sulfuric Acid,Nitric Acid; 5 H,0 - 5 °C
标题:Preparation Of New Biologically Active And Water Soluble Dyes: Characterization,Aggregation And Extraction Of Metal Ions From Solutions
作者:Touj,Nedra; Al-Ayed,Abdullah Sulaiman; Hamdi,Naceur
参考文献:Asian Journal Of Chemistry 日期:2019 卷标:31(6) 页码:1398-1404]
= 89-40-7
反应条件:1.1 Reagents: Sulfuric Acid,Nitric Acid; 30 Min,0 °C -> Rt1.2 Rt; 4 H,35 °C
标题:New Anthracene-Based-Phthalocyanine Semi-Conducting Materials: Synthesis And Optoelectronic Properties
作者:Kahouech,M. S.; Hriz,K.; Touaiti,S.; Bassem,J.
参考文献:Materials Research Bulletin 日期:2016 卷标:75 页码:144-154]
= 89-40-7
反应条件:1.1 Reagents: Sulfuric Acid,Nitric Acid Solvents: Water; 10 - 15 °C; 15 °C -> Rt; 16 H,Rt
标题:Synthesis And Spectral Properties Of Phthalimide Based Alkali-Clearable Azo Disperse Dyes
作者:Koh,Joonseok; Kim,Hoegyeong; Park,Jongseung
参考文献:Fibers And Polymers 日期:2008 卷标:9(2) 页码:143-151]
= 89-40-7
反应条件:1.1 Reagents: Sulfuric Acid,Nitric Acid Solvents: Water; 10 - 15 °C; 15 °C -> Rt; 16 H,Rt1.2 Reagents: Water; Cooled
标题:Synthesis And Spectroscopic Properties Of Novel Azo Dyes Derived From Phthalimide
作者:Choi,Jae-Hong; Park,Joon-Soo; Kim,Mi-Hyeon; Lee,Hyun-Young; Towns,Andrew D.
参考文献:Coloration Technology 日期:2007 卷标:123(6) 页码:379-386]
= 89-40-7
反应条件:1.1 Reagents: Sulfuric Acid,Fuming Nitric Acid; 10 °C -> 25 °C; 12 H,25 °C
标题:Synthesis Of Phthalimide Disperse Dyes And Study On The Interaction Energy
作者:Zhan,Yizhen; Zhao,Xue; Wang,Wei
参考文献:Dyes And Pigments 日期:2017 卷标:146 页码:240-250]
= 89-40-7
反应条件:1.1 Reagents: Sulfuric Acid,Nitric Acid; 12 H,10 °C -> 25 °C
标题:Synthesis And Application Of N-Butyl Substituted Phthalimide Disperse Dyes
作者:Zhao,Xue
参考文献:Textile Research Journal 日期:2019 卷标:89(15) 页码:3034-3047]
5466-84-2 = 89-40-7
反应条件:1.1 Reagents: Formamide
标题:Imidation Of Cyclic Carboxylic Anhydrides Under Microwave Irradiation
作者:Peng,Yanqing; Song,Gonghua; Qian,Xuhong
参考文献:Synthetic Communications 日期:2001 卷标:31(12) 页码:1927-1931]
= 89-40-7
反应条件:1.1 Reagents: Sulfuric Acid,Nitric Acid Solvents: Water; Rt
标题:The Design,Synthesis And In Vitro Immunosuppressive Evaluation Of Novel Isobenzofuran Derivatives
作者:Yang,Na; Wang,Qing-He; Wang,Wen-Qian; Wang,Jian; Li,Feng; Et Al
参考文献:Bioorganic & Medicinal Chemistry Letters 日期:2012 卷标:22(1) 页码:53-56]
= 89-40-7
反应条件:1.1 Reagents: Sulfuric Acid,Nitric Acid Solvents: Water; Rt -> 5 °C; 10 - 15 °C1.2 10 °C -> Rt; 10 H,Rt
标题:Synthesis Of 4-Nitrophthalimide
作者:Xiang,Bin; Shi,Hong-Xin; Jiang,Yi-Fei; Chen,Hua; Chen,Zhan-Zhi; Et Al
参考文献:Zhejiang Gongye Daxue Xuebao 日期:2003 卷标:31(5) 页码:512-514]
= 89-40-7
反应条件:1.1 Reagents: Sulfuric Acid,Nitric Acid; 30 Min,0 °C; 0 °C -> Rt1.2 4 H,35 °C
标题:Synthesis And Characterization Of New Zn-Phthalocyanine-Based Semi-Conducting Materials
作者:Touaiti,Sarra; Hajri,Amira; Kahouech,Mourad Shady; Khiari,Jameleddin; Jamoussi,Bassem
参考文献:Arabian Journal Of Chemistry 日期:2017 卷标:10]
= 89-40-7
反应条件:1.1 Reagents: Phosphorus Pentoxide,Sulfuric Acid Solvents: Water; Rt -> 5 °C1.2 Reagents: Sulfuric Acid,Nitric Acid Solvents: Water; < 10 °C; 10 °C -> Rt; 10 H,Rt1.3 Reagents: Water; Cooled
标题:New Process For 4-Aminophthalimide Synthesis
作者:Lu,Liang; Yang,Wenge; Hu,Yonghong
参考文献:Nanjing Gongye Daxue Xuebao 日期:2008 卷标:30(6) 页码:51-53]
= 89-40-7
反应条件:1.1 Reagents: Sulfuric Acid,Nitric Acid
标题:Synthesis Of Some Schiff Bases Derived From Copper Tetraaminophthalocyanines
作者:Isfan,Liliana; Tomas,Stefan; Pop,Cristina; Boscornea,Cristian; Mocanu-Ionescu,Roxana
参考文献:Revista De Chimie (Bucharest 日期:2007 卷标:58(7) 页码:664-668
邻苯二甲酸亚胺置于硫酸,硝酸体系中,化学反应 1.0H,以52%的收率获得产物4-硝基邻苯二甲酰亚胺
参考文献:基于pyr-吩嗪稠合的单酰亚胺和双酰亚胺的新型n沟道有机半导体
标题:基于pyr-吩嗪稠合的单酰亚胺和双酰亚胺的新型n沟道有机半导体
摘要:摘要通过亚胺缩合反应合成了大的π共轭pyr-吩嗪单酰亚胺和双酰亚胺.这些酰亚胺在溶液中自组装后会形成有序的1D纳米带.电化学和电导率测量表明,它可以用作n沟道半导体,其载流子迁移率高达4.1 Cm 2 V-1 S-1.两种烷基化的酰亚胺都具有高发光性,可以使用三氟乙酸通过质子化进行淬灭,可以用作潜在的比色酸传感器.
DOI:10.1016/j.Cclet.2017.09.015
专利信息
专利号:US-9428524-B2
优先权日:2010-05-25
标 题:Synthetic process for the manufacture of ecteinascidin compounds
发明人:MARTIN LÓPEZ MA JESÚS; FRANCESCH SOLLOSO ANDRÉS; CUEVAS MARCHANTE MARIA DEL CARMEN
权利人:MARTIN LÓPEZ MA JESÚS; FRANCESCH SOLLOSO ANDRÉS; CUEVAS MARCHANTE MARIA DEL CARMEN; PHARMA MAR SA
摘要:This invention relates to compounds of formula II: wherein R 1 , R 2 , Prot SH , and Prot NH are as defined, to processes for the synthesis of ecteinascidins of formula I from compounds of formula II, and to processes for the synthesis of compounds of formula II.
专利号:US-2003138376-A1
优先权日:2000-03-17
标题 :Dosing form for reagents, use of said dosing form in organic chemical synthesis and production of said dosing form
发明人:RUHLAND THOMAS; HOLM PER; SCHULTZ KIRSTEN; HOLM JANNIE EGESKOV; ANDERSEN KIM
权利人:LUNDBECK & CO AS H
摘要:A dosing form for at least one solid reagent for use in conventional organic and inorganic synthesis, in parallel synthesis, and in split and mix synthesis in combinatorial chemistry is provided as compressed tablets each containing the same predetermined amount of said at least one reagent embedded in a polymer matrix comprising beads of a polymer insoluble in the solvents for the intended synthesis, which tablets are capable of disintegrating in said solvent for release of the at least one reagent and disperse the matrix as polymer beads into the solvent. The polymer beads forming the matrix and the reagents of the dosing form can easily be removed by filtration in order to separate these from a formed soluble product. n In a method for producing the dosing form, beads of one or more polymers are mixed with the reagents and compressed into tablets after pre-treatment with an aprotic organic solvent.
专利号:US-8362234-B2
优先权日:2006-03-24
标题 :Solid support reagents for synthesis
发明人:HATALA PAUL J; KURZ MARKUS
权利人:ARCHEMIX LLC; HATALA PAUL J; KURZ MARKUS
摘要:The present invention relates to a compound according to the formula: n nwherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , Y, Z, n, s, and t are as defined herein. These compounds are useful for methods of solid phase synthesis.
专利号:US-RE41614-E
优先权日:1998-09-30
标题 :Synthetic analogs of ecteinascidin-743
发明人:COREY ELIAS J
权利人:HARVARD COLLEGE
摘要:The present invention is directed to the synthesis and characterization of compounds having the formula: n n wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 and R 9 are each independently selected from the group consisting of H, OH, OR′, SH, SR′, SOR′, SO 2 R′, NO 2 , NH 2 , NHR′, N(R′) 2 , NHC(â• O)R′ NHC( â• O ) R′ , CN, halogen, â• O, C(â• O)H, C(â• O)R′, CO 2 H, CO 2 R′, C 1 -C 12 alkyl, C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted aralkyl, and substituted or unsubstituted heteroaromatic; wherein each of the R′ groups is independently selected from the group consisting of H, OH, NH 2 , NO 2 , SH, CN, halogen, â• O, C(â• O)H, C(â• O)CH 3 , CO 2 H, CO 2 CH 3 , C 1 -C 12 alkyl, C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, aryl, aralkyl, and heteroaromatic; wherein each dotted circle represents one, two or three optional double bonds; wherein R 7 and R 8 may be are joined into a carbocyclic or heterocyclic ring system; and wherein X 1 and X 2 are each independently defined as above for R 1 -R 8 R 1 - R 6 and R 9 , an each further includes specific preferred groups as defined herein.
专利号:US-2005059817-A1
优先权日:2000-09-01
标题 :Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives
发明人:BEIGELMAN LEONID; KARPEISKY ALEXANDER; SEREBRYANY VLADMIR; HAEBERLI PETER; SWEEDLER DAVID
权利人:SIRNA THERAPEUTICS INC
摘要:The present invention provides methods for the chemical synthesis of nucleosides and derivatives thereof, including 2′-amino, 2′-N-phthaloyl, 2′-O-methyl, 2′-0-silyl, 2′-O-triisopropylsilyloxymethyl, 2′-OH nucleosides, C-nucleosides, nucleoside phosphoramidites, C-nucleoside phosphoramidites, and non-nucleoside derivatives.
专利号:US-6569859-B1
优先权日:2000-02-22
标题 :Synthetic analogs of ecteinascidin-743
发明人:COREY ELIAS J
权利人:HARVARD COLLEGE
摘要:The present invention is directed to the synthesis and characterization of compounds having the formula: n wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 and R 9 are each independently selected from the group consisting of H, OH, OR′, SH, SR′, SOR′, SO 2 R′, NO 2 , NH 2 , NHR′, N(R′) 2 , NHC(O)R′, CN, halogen, â• O, C(â• O)H, C(â• O)R′, CO 2 H, CO 2 R′, C 1 -C 12 alkyl, C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted aralkyl, and substituted or unsubstituted heteroaromatic; n wherein each of the R′ groups is independently selected from the group consisting of H, OH, NH 2 , NO 2 , SH, CN, halogen, â• O, C(â• O)H, C(â• O)CH 3 , CO 2 H, CO 2 CH 3 , C 1 -C 12 alkyl, C 2 -C 12 alkenyl, C 2 -C 12 alkynyl, aryl, aralkyl, and heteroaromatic; n wherein each dotted circle represents one, two or three optional double bonds; n wherein R 7 and R 8 may be joined into a carbocyclic or heterocyclic ring system; and n wherein X 1 and X 2 are each independently defined as above for R 1 -R 8 , and each furher includes specific preferred groups as defined herein.