CAS: 50529-33-4; 2-Chloro-1-Fluoro-4-Isocyanatobenzene

该化合物是一种有机化合物,其特点是,在苯环上有一个异丙氰酸盐功能组(-N=C=O),该组子进一步被氯原子和氟联苯组所取代,该组子的特点是无色的黄色液体或固态,视其具体形式和纯度而定,通常看起来无色,可粉黄液体或固态;已知该组子的活性,特别是由于异氰酸盐组的电益性质而增加的核生殖反应;氯和氟分成分的存在可影响其化学行为,包括其溶性及稳定性;在药物,农用化学品和其他精密化学品的合成中,经常使用这种化合物,因为其是一种重要的中间体;在处理该化合物时,安全防范措施至关重要,因为异丙酸盐可能有毒,对呼吸系统和皮肤产生刺激.应当遵循适当的储存和处理程序,以减轻任何潜在危害.

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3-chloro-4-fluorophenylamine bis(trichloromethyl) carbonate phosgene 3-(3-chloro-4-fluoro-phenyl)-6-methyl-[1,3]oxazine-2,4-dione 1,1-Dibutyl-3-(3-chloro-4-fluoro-phenyl)-urea

合成工艺路线路线简述

    📜3-氯-4-氟苯胺置于硫酸体系中,用 甲苯 作为反应溶剂,化学反应 2.0H,反应生成 异氰酸-3-氯-4-氟苯酯
    参考文献:Organosilicon Synthesis Of Isocyanates: I. Synthesis Of Isocyanates Of The Furan,Thiophene,And Mono-And Polyfluorophenyl Series
    标题:Organosilicon Synthesis Of Isocyanates: I. Synthesis Of Isocyanates Of The Furan,Thiophene,And Mono-And Polyfluorophenyl Series
    摘要:A Convenient Synthesis Of Known And Unknown Isocyanates Of The Furan,Thiophene,And Mono-And Polyfluorophenyl Series,Involving Silylation Of Starting Amines With Hexamethyldisilazane Or Chlorotrimethylsilane,Followed By Phosgenation Of The Resulting N-Silyl-Substituted Amines. An Unusual High-Temperature Rearrangement Of 3-(Methoxycarbonyl)-4,5-Dimethylthiophene-2-Yl Isocyanate Into Its 5-Ethyl Isomer. Ortho-Fluorine Substituent In Anilines Decreases The Yield Of Isocyanates,Whereas 2,3,5,6-Tetrafluorophenyl Isocyanate Exists For Only A Short Time As A 5% Toluene Solution.
    DOI:10.1134/s1070363206010208

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    专利信息


    专利号:EP-3515880-B1
    优先权日:2017-03-17
    标题:Methods and compositions for synthesis of encoded libraries
    发明人:LI JIN; MORGAN BARRY A; Wan jinqiao; DOU DENGFENG; LIU GUANSAI; CHANG YONG; CHEN QIUXIA; WANG XING; XU YANSHAN; HU DONGYAN; LIU JIAN; CHENG XUEMIN
    权利人:HITGEN INC

    专利号:US-2020149034-A1
    优先权日:2017-03-17
    标题:Methods and Compositions for Synthesis of Encoded Libraries

    专利号:US-4644010-A
    优先权日:1982-09-28
    标题:Certain β-oxo-α-carbamoylpyrrolepropionitriles
    发明人:WALKER GORDON N
    权利人:CIBA GEIGY CORP
    摘要:1-Unsubstituted β-oxo-α-(phenylcarbamoyl)-β-pyrrolylpropionitriles, e.g. those of the formula ##STR1## wherein R 1 and R 2 =H or alkyl, and R 3 and R 4 =H, alkyl, alkoxy, OH, halogen or CF 3 , are analgesic, and antiarthritic agents. Their synthesis, pharmaceutical compositions thereof, and methods of treatment utilizing such compounds are included.

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