CAS: 85068-32-2; 2-(3,5-Bis(Trifluoromethyl)Phenyl)Acetonitrile

该化合物是有机化合物,其特点是芳香结构,并有三氟甲基组;该化合物的特点是以三,五种基座替换的苯环,这大大增强了其电离脱色特性;丙硝基苯三烯功能组有助于其在极地溶剂中的再活性和溶解性;由于存在多种氟原子,该化合物具有独特的物理和化学特性,包括增加亲脂性和热稳定性;一般是淡黄色液体或固体无色,视温度和纯度而定;三氟甲基组还对该化合物的化学行为产生显著影响,使其在各种应用中有用,包括药物和农用化学品;此外,该化合物的结构可能会影响其在生物系统中的相互作用,从而引起对药用化学的兴趣;在处理和接触准则方面,应参考安全数据,因为氟化化合物可构成具体的健康和环境风险.

结构式图片

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

3,5-(bistrifluoromethyl)chlorobenzene cyanoacetic acid 3,6-bis(trifluoromethyl)bromobenzene sodium cyanoacetate cyclopentanecarbonitrile1-3,5-Bis(trifluoromethyl)phenylcyclopentanecarbonitrile (3,5-bis-trifluoromethylphenyl)-bromo-acetonitrile

合成工艺路线路线简述

  • 合成目标产物 3,5-Bis(Trifluoromethyl)Phenylacetonitrile 主要起始原料 3,5-Bis(Trifluoromethyl)Chlorobenzene And Cyanoacetic Acid
  • 328-70-1 = 85068-32-2
    反应条件:1.1 Reagents: Lithium Chloride Catalysts: Bis(1,5-Cyclooctadiene)Nickel,2-(1H-Imidazol-2-Yl)Pyridine,2,4,5,6-Tetra(9H-Carbazol-9-Yl)Isophthalonitrile Solvents: Dimethyl Sulfoxide; 16 H,55 °C
    标题:Photoinduced Nickel-Catalyzed Demethylative Cyanation And Decarboxylative Cyanomethylation Of Aryl Halides
    作者:Lee,Shao-Chi; Zhu,Chen; Huang,Kun; Bau,Jeremy A.; Jia,Jiaqi; Et Al
    参考文献:Acs Catalysis 日期:2023 卷标:13(24) 页码:16279-16285
在 甲醇体系中,化学反应生成 3,5-双(三氟甲基)苯乙腈
参考文献:Carbanion Reactivity; Kinetics Of The Reactions Of Benzyl Cyanide Anions With Aromatic Nitro-Compounds
标题:Carbanion Reactivity; Kinetics Of The Reactions Of Benzyl Cyanide Anions With Aromatic Nitro-Compounds
摘要:Rate And Equilibrium Measurements Are Reported For The Reactions In Methanol Of Carbanions Derived From 12 Ring-Substituted Benzyl Cyanides With 1,3,5-Trinitrobenzene To Give Sigma-Adducts. Some Data For Reaction Of The Carbanions With 4-Nitrobenzofuroxan Were Also Measured. With Increasing Carbanion Reactivity,Rate Constants Approach A Limit Of Just Below 10(9) Dm(3) Mol(-1) S(-1). Intrinsic Reactivities Of Carbanions In Sigma-Adduct Forming Transfer Reactions Are Compared.
DOI:10.1039/p29950000443

海关参考信息

专利信息


专利号:US-9428490-B2
优先权日:2011-07-29
标 题 :Nuclear transport modulators and uses thereof
发明人:SANDANAYAKA VINCENT P; SHACHAM SHARON; KAUFFMAN MICHAEL; SHECHTER SHARON; MCCAULEY DILARA; LANDESMAN YOSEF; SENAPEDIS WILLIAM; SAINT-MARTIN JEAN-RICHARD
权利人:SANDANAYAKA VINCENT P; SHACHAM SHARON; KAUFFMAN MICHAEL; SHECHTER SHARON; MCCAULEY DILARA; LANDESMAN YOSEF; SENAPEDIS WILLIAM; SAINT-MARTIN JEAN-RICHARD; KARYOPHARM THERAPEUTICS INC
摘要:The invention generally relates to nuclear transport modulators, e.g CRM1 inhibitors, and more particularly to a compound represented by formula (I): or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of structural formula (I), or a pharmaceutically acceptable salt or composition thereof, e.g, in the treatment, modulation and/or prevention of physiological conditions associated with CRM1 activity.
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合成参考文献


参考文献:10.1007/s10895-024-04016-w
摘要:Huang H, Pan S, Yuan B, Wang N, Shao L, Chen ZE, Zhang H, Huang WZ. Recent Research Progress of Benzothiazole Derivative Based Fluorescent Probes for Reactive Oxygen (H2O2 HClO) and Sulfide (H2S) Recognition. J Fluoresc. 2025 Aug;35(8):6225–42. doi: 10.1007/s10895-024-04016-w.
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