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di-n-butyldi-isopropenyltin | 1175711-35-9

中文名称
——
中文别名
——
英文名称
di-n-butyldi-isopropenyltin
英文别名
——
di-n-butyldi-isopropenyltin化学式
CAS
1175711-35-9
化学式
C14H28Sn
mdl
——
分子量
315.086
InChiKey
FFKAJPNFCDSCKU-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):
    4.85
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为产物:
    描述:
    2-溴丙烯二丁基二氯化锡magnesium 作用下, 以 not given 为溶剂, 生成 di-n-butyldi-isopropenyltin
    参考文献:
    名称:
    A novel mode of access to polyfunctional organotin compounds and their reactivity in Stille cross-coupling reaction
    摘要:
    Mono-, di-, tri- and tetra-functional organotin compounds were easily prepared in a sonicated Barbier reaction using ultrasound technology via coupling reaction of organo halides with tin halides (Bu3SnCl, Bu2SnCl2, BuSnCl3, SnCl4) mediated by magnesium metal. The di- and tri- functional organotin compounds were tested in a Stille cross-coupling reaction in order to ascertain how many groups were transferred. (C) 2009 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2009.03.030
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文献信息

  • A novel mode of access to polyfunctional organotin compounds and their reactivity in Stille cross-coupling reaction
    作者:Sandrine Lamandé-Langle、Mohamed Abarbri、Jérôme Thibonnet、Alain Duchêne
    DOI:10.1016/j.jorganchem.2009.03.030
    日期:2009.7
    Mono-, di-, tri- and tetra-functional organotin compounds were easily prepared in a sonicated Barbier reaction using ultrasound technology via coupling reaction of organo halides with tin halides (Bu3SnCl, Bu2SnCl2, BuSnCl3, SnCl4) mediated by magnesium metal. The di- and tri- functional organotin compounds were tested in a Stille cross-coupling reaction in order to ascertain how many groups were transferred. (C) 2009 Elsevier B.V. All rights reserved.
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