CAS: 1794-84-9; Chloronitromethane

该化合物是一种有机化合物,其特点是与甲烷主干柱相连的氯和硝基功能组,其特点是无色的黄色液体,其气味明显可见,它以水中中等溶性以及有机溶剂中较高溶性而著称,它可用于各种化学用途.氯硝基甲烷主要用作合成药物,农用化学品和其他有机化合物的中间体.它具有极地溶剂和相对较低的沸点等特性.由于氯和硝基化合物的存在,它可以参与一系列化学反应,包括核循环替代和减少.然而,必须谨慎地处理这种物质,因为它可能对健康造成危害,包括对皮肤,眼睛和呼吸系统造成刺激,而且如果浸入或吸入,可能有害.在与该化合物合作时,应注意适当的安全措施.

结构式图片

MSDS等安全信息

    上下游产品

    CAS号85915-53-3 Chloronitroacet... | CAS号82208-51-3 chloronitro-Ace... | CAS号663-08-1 2-nitro-3,3-dif... | CAS号75-52-5 硝基甲烷 | CAS号14011-27-9 ethyl 2-chloro-... | CAS号76-06-2 氯化苦 | CAS号186581-53-3 重氮甲烷 | CAS号34557-54-5 methane | CAS号623-73-4 重氮乙酸乙酯 | CAS号60-29-7 乙醚 | CAS号113-00-8 guanidine | CAS号21272-85-5 硝甲基苯砜 | CAS号1184-89-0 二溴一氯硝基甲烷 | CAS号66073-97-0 4-CHLOROBENZENE... | CAS号625-76-3 二硝甲烷 | CAS号62635-34-1 2-氯-2-硝基乙醇 | CAS号32349-14-7 2-chloro-2-nitr... | CAS号51351-89-4 4-(TOLUENESULPH...

    合成工艺路线路线简述

    • 合成目标产物 Chloronitromethane 主要起始原料 Propanoyl Chloride, 2,3-Dichloro-3,3-Difluoro-2-Nitro-
    • (文献来源)合成步骤主要原料 Propanoyl Chloride, 2,3-Dichloro-3,3-Difluoro-2-Nitro-
    📜氯硝基乙酰氯置于水体系中,用 乙醚 用作溶剂,化学反应生成氯硝甲烷
    参考文献:Synthesis Of Chloro-And Dichloronitromethanes
    标题:Synthesis Of Chloro-And Dichloronitromethanes
    摘要:
    Doi:10.1007/bf00954250

    海关参考信息

    专利信息


    专利号:US-6198000-B1
    优先权日:1997-07-07
    标 题:Intermediates useful in the synthesis of quinoline antibiotics
    发明人:HAWKINS JOEL M
    权利人:PFIZER
    摘要:A process for preparing a compound of the formula n wherein R 1 , m, o and p are described below, which comprises adding a base of the formula n wherein R 2 , R 3 and R 4 are as described below, to a solution comprising a compound of the formula n wherein R 1 , m, o and p are as described below, and a halonitromethane of the formula O 2 NCH 2 X, wherein X is a halogen atom dissolved in a non-aqueous inert solvent. The compounds of formula III are useful as intermediates in the syntheses of azabicyclo quinoline carboxylic acids, and their pharmaceutically acceptable salts and prodrugs, having antibacterial activity. This invention also relates to the base of formula IV wherein each R 2 is butyl, R 3 is hydrogen and each R 4 is t-butyl.

    专利号:US-5298629-A
    优先权日:1992-03-02
    标题 :Intermediates in the synthesis of quinoline antibiotics
    发明人:BRAISH TAMIN F
    权利人:PFIZER
    摘要:This invention relates to compounds of the formulae ##STR1## wherein R and X are defined as below. These compounds are useful as intermediates in the syntheses of azabicyclo quinoline carboxylic acids having antibacterial activity.

    专利号:US-6057455-A
    优先权日:1996-07-09
    标题 :Preparation of intermediates useful in the synthesis of quinoline antibiotics
    发明人:HAWKINS JOEL M
    权利人:PFIZER
    摘要:A process for preparing a compound of the formula ##STR1## wherein R 1 , m, o and p are described below, which comprises adding a base of the formula ##STR2## wherein R 2 , R 3 and R 4 are as described below, to a solution comprising a compound of the formula ##STR3## wherein R 1 , m, o and p are as described below, and a halonitromethane of the formula O 2 NCH 2 X, wherein X is a halogen atom dissolved in a non-aqueous inert solvent. The compounds of formula III are useful as intermediates in the syntheses of azabicyclo quinoline carboxylic acids, and their pharmaceutically acceptable salts and prodrugs, having antibacterial activity. This invention also relates to the base of formula IV wherein each R 2 is butyl, R 3 is hydrogen and each R 4 is t-butyl.

    专利号:EP-0818445-A1
    优先权日:1996-07-09
    标 题 :Preparation of intermediates useful in the synthesis of quinoline antibiotics
    发明人:HAWKINS JOEL MICHAEL
    权利人:PFIZER
    摘要:A process for preparing a compound of the formulan nwherein R 1 , m, o and p are described below, which comprises adding a base of thenformulan nwherein R 2 , R 3 and R 4 are as described below, to a solution comprising a compoundnof the formula n nwherein R 1 , m, o and p are as described below, and a halonitromethane of the formulanO 2 NCH 2 X, wherein X is a halogen atom dissolved in a non-aqueous inert solvent.nThe compounds of formula III are useful as intermediates in the syntheses of azabicyclonquinoline carboxylic acids, and their pharmaceutically acceptable salts and prodrugs,nhaving antibacterial activity. This invention also relates to the base of formula IVnwherein each R 2 is butyl, R 3 is hydrogen and each R 4 is t -butyl.

    专利号:US-5256791-A
    优先权日:1992-03-02
    标 题 :Preparation of intermediates in the synthesis of quinoline antibiotics

    专利号:CN-1076440-A
    优先权日:1992-03-02
    标题:Preparation of intermediates in the synthesis of quinoline antibiotics

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:H. G. Adolph and M. J. Kamlet, J. Am. Chem. Soc. 88, 4761 (1966).
    参考文献:10.1021/jp061100f
    摘要:Shen Q, Brown JW, Malona JA, Cochran JC, Richardson AD. Molecular structure and conformation of chloronitromethane as determined by gas-phase electron diffraction and theoretical calculations. J Phys Chem A. 2006 Jun 15;110(23):7491–5. doi: 10.1021/jp061100f.
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