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1H,1H,2H,2H-perfluorooctyltriallylsilane | 193828-95-4

中文名称
——
中文别名
——
英文名称
1H,1H,2H,2H-perfluorooctyltriallylsilane
英文别名
Tri(prop-2-en-1-yl)(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)silane;tris(prop-2-enyl)-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)silane
1H,1H,2H,2H-perfluorooctyltriallylsilane化学式
CAS
193828-95-4
化学式
C17H19F13Si
mdl
——
分子量
498.403
InChiKey
NTSTZKPGQWYESW-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):
    8.12
  • 重原子数:
    31
  • 可旋转键数:
    13
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    13

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1H,1H,2H,2H-perfluorooctyltriallylsilane硼烷sodium hydroxide双氧水 作用下, 以 四氢呋喃 为溶剂, 反应 5.0h, 以76%的产率得到
    参考文献:
    名称:
    Synthesis of perfluoroalkyl-containing multifunctional groups compounds for textile finishing
    摘要:
    A new kind of perfluoroalkyl-containing multifunctional groups compound was designed. Treatment of 1H,1H,2H,2H-perfluorooctyltrichlorosilane (4) with allylmagnesium bromide provided key intermediate 1H,1H,2H,2H-perfluorooctyltriallylsilane (2). Hydroboration followed by oxidation, epoxidation and dihydroxylation of 2 gave perfluoroalkyl-containing multifunctional groups compound 1a, 1b and 1c, respectively. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0022-1139(01)00495-x
  • 作为产物:
    描述:
    1H,1H,2H-全氟-1-辛烯 在 chloroplatinic acid 1,1,3,3-tetramethyl-1,3-divinyldisiloxane complex 三氯硅烷magnesium 作用下, 以 乙醚 为溶剂, 反应 30.0h, 生成 1H,1H,2H,2H-perfluorooctyltriallylsilane
    参考文献:
    名称:
    Synthesis of perfluoroalkyl-containing multifunctional groups compounds for textile finishing
    摘要:
    A new kind of perfluoroalkyl-containing multifunctional groups compound was designed. Treatment of 1H,1H,2H,2H-perfluorooctyltrichlorosilane (4) with allylmagnesium bromide provided key intermediate 1H,1H,2H,2H-perfluorooctyltriallylsilane (2). Hydroboration followed by oxidation, epoxidation and dihydroxylation of 2 gave perfluoroalkyl-containing multifunctional groups compound 1a, 1b and 1c, respectively. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0022-1139(01)00495-x
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文献信息

  • Synthesis of perfluoroalkyl-containing multifunctional groups compounds for textile finishing
    作者:Feng-Ling Qing、Min Ji、Ronghua Lu、Kelu Yan、Zhiping Mao
    DOI:10.1016/s0022-1139(01)00495-x
    日期:2002.1
    A new kind of perfluoroalkyl-containing multifunctional groups compound was designed. Treatment of 1H,1H,2H,2H-perfluorooctyltrichlorosilane (4) with allylmagnesium bromide provided key intermediate 1H,1H,2H,2H-perfluorooctyltriallylsilane (2). Hydroboration followed by oxidation, epoxidation and dihydroxylation of 2 gave perfluoroalkyl-containing multifunctional groups compound 1a, 1b and 1c, respectively. (C) 2002 Elsevier Science B.V. All rights reserved.
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