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

6-iodo-1-decene | 152500-75-9

中文名称
——
中文别名
——
英文名称
6-iodo-1-decene
英文别名
6-Iododec-1-ene
6-iodo-1-decene化学式
CAS
152500-75-9
化学式
C10H19I
mdl
——
分子量
266.165
InChiKey
BWEZRTBTOKHMGG-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):
    5.6
  • 重原子数:
    11
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    有机锌试剂的分子内碳金属化。
    摘要:
    伯或仲烯基锌的分子内环化反应在高度敏感的功能下,在完全区域特异性的5-exo-trig环化中导致环戊基甲基锌衍生物。
    DOI:
    10.1016/s0040-4020(01)85661-1
  • 作为产物:
    描述:
    5-溴-1-戊烯咪唑magnesium三苯基膦 作用下, 反应 3.08h, 生成 6-iodo-1-decene
    参考文献:
    名称:
    有机锌试剂的分子内碳金属化。
    摘要:
    伯或仲烯基锌的分子内环化反应在高度敏感的功能下,在完全区域特异性的5-exo-trig环化中导致环戊基甲基锌衍生物。
    DOI:
    10.1016/s0040-4020(01)85661-1
点击查看最新优质反应信息

文献信息

  • Intramolecular Carbozincation of Unactivated Alkenes Occurs through a Zinc Radical Transfer Mechanism
    作者:Theodore Cohen、Heather Gibney、Roman Ivanov、Edmund A.-H. Yeh、Ilan Marek、Dennis P. Curran
    DOI:10.1021/ja076554k
    日期:2007.12.1
    The cyclizations of a number of terminally unsaturated alkenyl zinc iodides to cyclopentylmethylzinc iodides, formerly believed to be nonradical in nature, have been revealed as radical chain cyclizations initiated by adventitious oxygen. Five cases are presented in which the published carbozincation cis/trans selectivities are essentially the same as those found for the cyclizations of the unsaturated alkyl iodide precursors of the, alkylzinc iodides by the iodine atom transfer method at approximately the same temperatures. In addition, it has been found that one of the organozinc cyclizations does not occur in a system in which oxygen has been rigorously excluded. The combined findings strongly suggest that these organozinc cyclizations occur by a zinc radical transfer mechanism rather than by a conventional carbometallation that is thought to occur with the analogous organolithium and organomagnesium cyclizations.
  • Intramolecular carbometallation of secondary organozinc reagents.
    作者:Christophe Meyer、Ilane Marek、Gilles Courtemanche、Jean-F. Normant
    DOI:10.1016/s0040-4039(00)61725-2
    日期:1993.9
    The intramolecular carbocyclization of secondary organozinc derivatives allows the preparation of cis-substituted cyclopentylmethylzinc derivatives in an easy and straightforward way.
  • Meyer Christophe, Marek Ilane, Courtemanche Gilles, Normant Jean-F., Tetrahedron, 50 (1994) N 40, S 11665-11692
    作者:Meyer Christophe, Marek Ilane, Courtemanche Gilles, Normant Jean-F.
    DOI:——
    日期:——
查看更多