CAS: 1632-84-4; 4-(Methylthio)Phenylisocyanate

该化合物是一种有机化合物,其特征是附于一个苯环的异丙氰酸酯功能组(-N=C=O),该元素组又被一个甲基硫磷组(-S-CH3)所取代.该化合物一般是无色的,以其浓厚,不浓的气味闻名而可见,在有机溶剂中溶解,但在水中溶解有限,异丙酸酯组的存在使其高度反应性,特别是核素,这可能导致尿素和其他衍生物的形成.这种再活动是其应用中的一个关键特征,特别是在各种药物和农用化学品合成中.此外,4-(甲基乙基)异丙酸盐酯被认为具有危险性,因为它可引起皮肤,眼睛和呼吸系统刺激,因此在处理和使用过程中必须采取适当的安全措施.

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CAS号123-09-1 4-氯茴香硫醚 | CAS号917-61-3 氰酸钠 | CAS号86764-40-1 1,1-dibenzyl-3-...

合成工艺路线路线简述

    📜N-Hydroxy-4-Methylsulfanylbenzamide置于carbonyldiimidazole体系中,用 乙腈 用作溶剂,化学反应 0.5H,反应生成异氰酸-4(甲硫基)苯酯
    参考文献:羰基二咪唑介导的丢失重排
    标题:羰基二咪唑介导的丢失重排
    摘要:发现羰基二咪唑(cdi)介导各种异羟肟酸的洛森重排为异氰酸酯.该过程在实验上是简单且温和的,咪唑和co 2是唯一的化学计量副产物.对于大规模应用而言意义重大,该方法避免了使用有害试剂,因此是curtius和hofmann重排标准处理条件的绿色替代方案.
    Doi:10.1021/ol9023387

    海关参考信息

    专利信息


    专利号:WO-9700244-A1
    优先权日:1995-06-19
    标题 :Process for parallel synthesis of a non-peptide library
    发明人:FRITZ JAMES E; KALDOR STEPHEN W
    权利人:LILLY CO ELI; FRITZ JAMES E; KALDOR STEPHEN W
    摘要:A process for the sequential preparation of a library of compounds having pharmaceutical usage. The process involves the sequential mixing of solution phase reagents, followed by scavenging of excess unreacted reagents with solid phase scavenging agents. The process is highly iterative and applicable for producing various ureas, thiureas, amides, carbonates and tertiary amines.

    专利号:US-2008280877-A1
    优先权日:2007-05-10
    标 题:Azetidines
    发明人:DACK KEVIN NEIL; SKERRATT SARAH ELIZABETH; YEAP SIEW KUEN
    权利人:PFIZER
    摘要:The invention relates to EP2 antagonist azetidines of formula (I) n n n n n n n n n n wherein Ar, R 1 , X, and Z are as defined herein, to their use in medicine, particularly in the treatment of endometriosis and/or uterine fibroids, to intermediates useful in their synthesis, and to compositions containing them.

    专利号:RU-2170231-C2
    优先权日:1994-09-29
    标 题:Imidazolidines substituted with heterocycle, method of their synthesis and pharmaceutical compositions containing thereof

    专利号:KR-19980076014-A
    优先权日:1997-04-04
    标 题 :Synthesis method of hydridein derivative using solution phase and solid phase reaction

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1055/s-2007-984534
    摘要:Papot S, Thomas M, Gesson J. Efficient Regio- and Stereoselective Synthesis of 1-β-O-Glucuronyl Carbamates and Carbonates from Unprotected 1,2,3,4-Hydroxyl Glucuronates. Synlett. 2007 Jul;2007(12):1966–8. doi: 10.1055/s-2007-984534.
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