摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

gem-dichlorocyclopropanol | 42039-22-5

中文名称
——
中文别名
——
英文名称
gem-dichlorocyclopropanol
英文别名
dichlorocyclopropanol;1-Hydroxy-2,2-dichlor-cyclopropan;2,2-Dichlorocyclopropan-1-ol
gem-dichlorocyclopropanol化学式
CAS
42039-22-5
化学式
C3H4Cl2O
mdl
——
分子量
126.97
InChiKey
MYGKOTXRVZHQSU-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    6
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    gem-dichlorocyclopropanol二苯并-18-冠醚-6 作用下, 以 乙醇 为溶剂, 以58%的产率得到吡唑
    参考文献:
    名称:
    Preparation of pyrazoles and pyrazolines by the reaction of chlorocyclopropanols with hydrazines in the presence of crown ethers
    摘要:
    DOI:
    10.1007/bf01157367
  • 作为产物:
    描述:
    1,1-Dichlor-2-trimethylsiloxy-cyclopropan盐酸 作用下, 以 四氢呋喃 为溶剂, 以100%的产率得到gem-dichlorocyclopropanol
    参考文献:
    名称:
    Inactivation of S-adenosylhomocysteine hydrolase with haloethyl and dihalocyclopropyl esters derived from homoadenosine-6′-carboxylic acid
    摘要:
    In a search for new inhibitors that exploit 5'-6' `hydrolytic activity' of AdoHcy hydrolase, a new series of haloethyl and dihalocyclopropyl esters 2-3 were designed and their interaction with the enzyme studied. Incubation of the enzyme with 2-3 resulted in time- and concentration-dependent inactivation of AdoHcy hydrolase as well as almost total depletion of its NAD+ content. Further results indicated that the `oxidative' but not the `hydrolytic' activity was involved in the inactivation process. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2004.09.050
点击查看最新优质反应信息

文献信息

  • Mechanism-based inactivation of α-chymotrypsin
    作者:Tsuyoshi Ohba、Naoki Tsuchiya、Kuniko Nishimura、Eitatsu Ikeda、Jun Wakayama、Hisashi Takei
    DOI:10.1016/0960-894x(96)00065-0
    日期:1996.3
    The peptidyl ester derivatives of 2,2-dichlorocyclopropanol and the amide derivative of 2,2-dichlorocyclopropylamine were prepred as novel mechanism-based inactivators of alpha-chymotrypsin. The esters inactivated alpha-chymotrypsin irreversibly but the amide did not show any irreversible inhibitory activity toward alpha-chymotrypsin.
  • SHOSTAKOVSKIJ, S. M.;MOCHALOV, V. N.;VOROPAEVA, T. K.;SHOSTAKOVSKIJ, V. M+, IZV. AN CCCP. CEP. XIM., 1985, N 1, 231-233
    作者:SHOSTAKOVSKIJ, S. M.、MOCHALOV, V. N.、VOROPAEVA, T. K.、SHOSTAKOVSKIJ, V. M+
    DOI:——
    日期:——
查看更多