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methyl (E)-4-bromo-2-octenoate | 137258-02-7

中文名称
——
中文别名
——
英文名称
methyl (E)-4-bromo-2-octenoate
英文别名
methyl (E)-4-bromooct-2-enoate
methyl (E)-4-bromo-2-octenoate化学式
CAS
137258-02-7
化学式
C9H15BrO2
mdl
——
分子量
235.121
InChiKey
PZBZIEUPWPJDEA-VOTSOKGWSA-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):
    3
  • 重原子数:
    12
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

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文献信息

  • Aerobic conversion of organic halides to alcohols. An oxygenative radical cyclization
    作者:Eiichi Nakamura、Tsuyoshi Inubushi、Satoshi Aoki、Daisuke Machii
    DOI:10.1021/ja00023a076
    日期:1991.11
  • TRIPTOLIDE DERIVATIVES AND PREPARATION METHOD AND USE THEREOF
    申请人:Hong Kong Baptist University
    公开号:US20160362691A1
    公开(公告)日:2016-12-15
    Tripyolide-nucleic acid aptamer derivatives, a preparation method and use thereof are shown. The structure of the triptolide-nucleic acid aptamer derivatives is as shown by formula I, wherein the definitions of R 1 -R 7 , G, A, B, M, Z and X are described. The present invention uses a nucleic acid aptamer and triptolide or modified compounds thereof as the starting materials, and introduces a linking group A at the C-14 hydroxyl group, epoxy groups and five-membered ring lactones in triptolide, then connects it to a nucleic acid aptamer B, and obtains the triptolide-nucleic acid aptamer derivatives. The triptolide-nucleic acid aptamer derivatives of the present invention have the characteristics of good targeting, a high anti-cancer activity, low toxicity and side effects, good water solubility and high bioavailability, and the preparation method of the present invention is scientific and reasonable and has a controllable quality and good repeatability, and is thereby suitable for production.
  • US9809822B2
    申请人:——
    公开号:US9809822B2
    公开(公告)日:2017-11-07
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