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7-Iodooct-7-ene-1,5-diol | 1260168-32-8

中文名称
——
中文别名
——
英文名称
7-Iodooct-7-ene-1,5-diol
英文别名
——
7-Iodooct-7-ene-1,5-diol化学式
CAS
1260168-32-8
化学式
C8H15IO2
mdl
——
分子量
270.11
InChiKey
WNFAZANMZMVNTI-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):
    2
  • 重原子数:
    11
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    7-Iodooct-7-ene-1,5-diol乙酸酐吡啶 作用下, 以 乙醚 为溶剂, 以287 mg的产率得到7-iodooct-7-ene-1 5-diyl diacetate
    参考文献:
    名称:
    One-pot sequential deoximation and allylation reactions of aldoximes in aqueous solution
    摘要:
    A simple procedure has been developed for conducting tin-mediated deoximation and allylation reactions of aldoximes in water to form homoallylic alcohols. Employing the new conditions, various homoallylic alcohols were produced in good to excellent yields. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.01.074
  • 作为产物:
    描述:
    3-bromo-2-iodoprop-1-ene5-羟基戊醛肟盐酸tin 、 titanium(III) chloride 、 作用下, 以 四氢呋喃 为溶剂, 生成 7-Iodooct-7-ene-1,5-diol
    参考文献:
    名称:
    One-pot sequential deoximation and allylation reactions of aldoximes in aqueous solution
    摘要:
    A simple procedure has been developed for conducting tin-mediated deoximation and allylation reactions of aldoximes in water to form homoallylic alcohols. Employing the new conditions, various homoallylic alcohols were produced in good to excellent yields. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.01.074
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文献信息

  • Tin Mediated Allylation Reactions of Enol Ethers in Water
    作者:Mei-Huey Lin、Shiang-Fu Hung、Long-Zhi Lin、Wen-Shing Tsai、Tsung-Hsun Chuang
    DOI:10.1021/ol102825t
    日期:2011.1.21
    Under tin-mediated Barbier-type reaction conditions, hydration of enol ethers takes place to form aldehydes that undergo allylation reactions. By using this process, various homoallylic alcohols and 2-halohomoallylic alcohols are produced in good to excellent yields.
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