CAS: 968-39-8; (Ethoxymethanetriyl)Tribenzene

该化合物是有机化合物,其独特结构特征为有机化合物,具有与三个苯环相连的中央乙氧基乙基乙基基组,该化合物具有芳香化合物的典型特性,如稳定性和接受电益替代反应的能力.乙氧基组的存在有助于其在有机溶剂中的溶解性,并可能影响其反应和与其他化学物种的互动.分子结构表明材料科学中的潜在应用,特别是在有机半导体的开发或作为前分子化学的建筑块.此外,该化合物的芳香性质可能具有有趣的光学特性,使其有可能用于染料或颜料中.然而,有必要详细研究其物理和化学特性,如熔点,沸点和再活性,以便充分了解其在各种化学环境中的行为.

英文名称(Ethoxymethanetriyl)Tribenzene
中文名称乙基三苯甲基醚
IUPAC名称(ethoxymethanetriyl)tribenzene
其它别名Ethyltritylether; (Trityloxy)Ethane; [ethoxy(Diphenyl)Methyl]Benzene; Clotrimazole Impurity 11; Ethyl Triphenylmethyl Ether; Clotrimazole Impurity 1; Triphenylmethylethylether; (Ethoxymethanetriyl)Tribenzene
CAS编号968-39-8
MFCD编号:MFCD00026925
EINECS号:635-557-4
分子式:C21H20O
分子量:288.39
产品CID: 2019028
产品分类分析化学 → 标准品 → 药典标准品和杂质标准品

相似结构搜索
InChIKey: HEXJOZGCQASJOM-UHFFFAOYSA-N
InChI=1S/C21H20O/c1-2-22-21(18-12-6-3-7-13-18,19-14-8-4-9-15-19)20-16-10-5-11-17-20/h3-17H,2H2,1H3…
计算化学: 氢键受体数1.0氢键供体数0.0可旋转键数5.0

MSDS等安全信息

危险类别水生慢性毒性类别4
危险描述H413 |可能对水生生物造成长期有害影响.
防范说明P273, and P501

欧盟法规

ECHA物质C&L通报

上下游产品

合成工艺路线路线简述

76-83-5 = 968-39-8
反应条件:1.1 Reagents: Sodium Bicarbonate; 12 H,50 °C
标题:A Self-Assembled Cage With Endohedral Acid Groups Both Catalyzes Substitution Reactions And Controls Their Molecularity
作者:Bogie,Paul M.; Holloway,Lauren R.; Ngai,Courtney; Miller,Tabitha F.; Grewal,Divine K.; Et Al
参考文献:Chemistry - A European Journal 日期:2019 卷标:25(43) 页码:10232-10238]

596-31-6 = 968-39-8
反应条件:1.1 Catalysts: Ceric Ammonium Nitrate Solvents: Ethanol
标题:Catalytic And Efficient Cleavage Of Allylic And Tertiary Benzylic Ethers And Esters With Ce(Iv)
作者:Iranpoor,Nasser; Mottaghinejad,Enayatolah
参考文献:Tetrahedron 日期:1994 卷标:50(24) 页码:7299-306]

132277-76-0 = 968-39-8 [标题:Reaction Conditions
标题:Single-Electron-Transfer-Initiated Thermal Reactions Of Arylmethyl Halides. Part 15. The Reaction Of Triphenylmethyl Bromide With Potassium O-Ethyl Dithiocarbonate (Potassium Xanthate) In Benzene And Cumene. A Note Of Caution On The Application Of The Radical Trap Dicyclohexylphosphine As A Probe For Electron-Transfer-Initiated Reactions Of Triphenylmethyl Halides
作者:Huszthy,Peter; Izso Gergacz,Gyongyi; Lempert,Karoly; Gyor,Miklos; Rockenbauer,Antal
参考文献:Journal Of The Chemical Society 日期:1990 卷标:(1990) 页码:2009-15]

538-51-2 + 1600-49-3 = 968-39-8 + 4553-59-7 + 1918941-25-9
反应条件:1.1 Catalysts: P-Toluenesulfonic Acid Solvents: Ethanol,Dichloromethane; 1 H,Rt
标题:Trityl Isocyanide As A Mechanistic Probe In Multicomponent Chemistry: Walking The Line Between Ugi- And Strecker-Type Reactions
作者:Cioc,Razvan C.; Preschel,Hans D.; Van Der Heijden,Gydo; Ruijter,Eelco; Orru,Romano V. A.
参考文献:Chemistry - A European Journal 日期:2016 卷标:22(23) 页码:7837-7842]

87839-57-4 = 968-39-8
反应条件:1.1 Solvents: 1,2-Dichloroethane
标题:Regioselective N- Or O-Tritylation Of 2(1H)-Pyridone - (Triphenylmethyl)Pyridones As Tritylation Agents
作者:Effenberger,Franz; Brodt,Werner; Zinczuk,Juan
参考文献:Chemische Berichte 日期:1983 卷标:116(9) 页码:3011-26]

50653-07-1 = 968-39-8
反应条件:1.1 Catalysts: Trimethylsilyl Triflate
标题:Trimethysilyl Triflate In Organic Synthesis. Part 11
作者:Noyori,R.; Murata,S.; Suzuki,M.
参考文献:Tetrahedron 日期:1981 卷标:37(23) 页码:3899-910]

= 968-39-8 [标题:Reaction Conditions
标题:Novel Synthesis Of Some Mixed Arylmethylalkyl Ethers
作者:Rutherford,Kenneth G.; Mamer,O. A.; Prokipcak,Joseph M.; Jobin,R. A.
参考文献:Canadian Journal Of Chemistry 日期:1966 卷标:44(19) 页码:2337-9]

76-83-5 = 968-39-8 + 119-61-9 + 76-84-6
反应条件:1.1 Reagents: Oxygen Solvents: Tert-Butylbenzene1.2 Reagents: Sodium Ethoxide
标题:Single Electron Transfer Initiated Thermal Reactions Of Arylmethyl Halides. Part 14. The Reaction Of Triphenylmethyl Halides With Tributylphosphine And Tributylamine In Apolar Solvents
作者:Huszthy,Peter; Izso Gergacz,Gyongyi; Lempert,Karoly; Kajtar-Peredy,Maria; Gyor,Miklos; Et Al
参考文献:Journal Of The Chemical Society 日期:1989 卷标:(1989) 页码:1513-20]

76-83-5 = 968-39-8 [标题:Reaction Conditions
标题:The Rates Of Alcoholysis Of Triarylmethyl Chlorides
作者:Nixon,A. C.; Branch,G. E. K.
参考文献:Journal Of The American Chemical Society 日期:1936 卷标:58 页码:492-8]

76-83-5 = 968-39-8
反应条件:1.1 7 H,150 °C
标题:New Reaction Of Organic Monohalides With Orthoformates
作者:Gazizov,M. B.; Ibragimov,Sh. N.; Khamidullina,O. D.; Karimova,R. F.; Pudovik,M. A.; Et Al
参考文献:Russian Journal Of General Chemistry 日期:2005 卷标:75(8) 页码:1325-1326]

76-84-6 = 968-39-8
反应条件:1.1 Catalysts: P-Toluenesulfonic Acid Solvents: Ethanol; Rt; Rt -> 78 °C; 30 Min,78 °C
标题:Microwave Assisted Transformation Of Compounds Capable Of Internal Reorientation
作者:Bednarz,Szczepan; Bogdal,Dariusz
参考文献:Proceedings Of The International Electronic Conference On Synthetic Organic Chemistry 日期:2007 卷标:(2007)]

87268-78-8 = 968-39-8
反应条件:1.1 Solvents: Ethanol; 4 H,Reflux1.2 Reagents: Sodium Hydroxide Solvents: Water
标题:Tetrazoles: Xliv. Synthesis And Chemical Properties Of 5-Substituted 2-Triphenylmethyltetrazoles
作者:Myznikov,L. V.; Artamonova,T. V.; Bel'Skii,V. K.; Stash,A. I.; Skvortsov,N. K.; Et Al
参考文献:Russian Journal Of Organic Chemistry (Translation Of Zhurnal Organicheskoi Khimii) 日期:2002 卷标:38(9) 页码:1360-1369]

76-83-5 = 968-39-8
反应条件:1.1 Reagents: Triethylamine Solvents: Ethanol1.2 Solvents: Methanol
标题:Reductive Demercuration In Deprotection Of Trityl Thioethers,Trityl Amines,And Trityl Ethers
作者:Maltese,M.
参考文献:Journal Of Organic Chemistry 日期:2001 卷标:66(23) 页码:7615-7625]

76-83-5 = 968-39-8
反应条件:1.1 Reagents: 1,8-Diazabicyclo[5.4.0]Undec-7-Ene Solvents: Dichloromethane; 24 H,Rt
标题:Iodine-Catalyzed Disproportionation Of Aryl-Substituted Ethers Under Solvent-Free Reaction Conditions
作者:Jereb,Marjan; Vrazic,Dejan
参考文献:Organic & Biomolecular Chemistry 日期:2013 卷标:11(12) 页码:1978-1999]

76-84-6 = 968-39-8 [标题:Reaction Conditions
标题:Synthesis Of Dialkyl Ethers By Substitution
作者:Tsukamoto,M.; Kitamura,M.
参考文献:Science Of Synthesis 日期:2008 卷标:37 页码:47-97]

50653-07-1 = 968-39-8
反应条件:1.1 Catalysts: Trimethylsilyl Triflate
标题:Trialkylsilyl Triflates In Organic Synthesis. Part 10. A Facile Procedure For O-Tritylation
作者:Murata,S.; Noyori,R.
参考文献:Tetrahedron Letters 日期:1981 卷标:22(22) 页码:2107-8]

= 968-39-8 [标题:Reaction Conditions
标题:Triaryl Methane Derivatives As Antiproliferative Agents
作者:Al-Qawasmeh,Raed A.; Lee,Yoon; Cao,Ming-Yu; Gu,Xiaoping; Vassilakos,Aikaterini; Et Al
参考文献:Bioorganic & Medicinal Chemistry Letters 日期:2004 卷标:14(2) 页码:347-350]

= 968-39-8 [标题:Reaction Conditions
标题:Esters Of Tertiary Alcohols
参考文献:Japan]

= 968-39-8 [标题:Reaction Conditions
标题:A Rapid,Simple,And Mild Procedure For Alkylation Of Phenols,Alcohols,Amides,And Acids
作者:Johnstone,Robert A. W.; Rose,Malcolm E.
参考文献:Tetrahedron 日期:1979 卷标:35(18) 页码:2169-73]

= 968-39-8 [标题:Reaction Conditions
标题:Interaction Of Tetraalkoxysilanes With Stable Carbonium Ions
作者:Kursanov,D. N.; Parnes,Z. N.; Kolomnikova,G. D.; Tyulyaev,I. I.
参考文献:Izvestiya Akademii Nauk Sssr 日期:1972 卷标:(1972) 页码:678-80

三苯基硫氯甲烷置于sodium Carbonate,Copper Dichloride体系中,用四氢呋喃作为反应溶剂,化学反应 15.0H,反应生成乙基三苯甲基醚
参考文献:Studies On The Development Of The Tritylsulfenyl Group As A Nitrogen Protecting Group And Application In A Synthesis Of .Delta.-Coniceine
标题:Studies On The Development Of The Tritylsulfenyl Group As A Nitrogen Protecting Group And Application In A Synthesis Of .Delta.-Coniceine
摘要:
DOI:10.1021/jo00168A032

海关参考信息

2902300000-甲苯
2906210000-苄醇
2901100000-饱和无环烃
2909199090-其他醚及其衍生物
💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
详情请参考：📖 海关编码查询和海关进出口税则

专利信息

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发明人：MARAS NENED; ZUPANCIC BORUT
权利人:MARAS NENED; ZUPANCIC BORUT; LEK PHARMACEUTICALS
摘要:The present invention relates to the field of organic synthesis and describes the synthesis of specific triazolopyrimidine compounds and intermediates thereof as well as related derivatives, suitable for the preparation of Ticagrelor (TCG).

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优先权日:1993-01-08
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