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Deca-1,3,5-triynyl-triisopropyl-silane | 920282-88-8

中文名称
——
中文别名
——
英文名称
Deca-1,3,5-triynyl-triisopropyl-silane
英文别名
Deca-1,3,5-triynyl-tri(propan-2-yl)silane
Deca-1,3,5-triynyl-triisopropyl-silane化学式
CAS
920282-88-8
化学式
C19H30Si
mdl
——
分子量
286.533
InChiKey
YYCXKPRHQVRBFZ-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

物化性质

  • 沸点:
    344.9±25.0 °C(Predicted)
  • 密度:
    0.871±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    20
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.68
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

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:
    参考文献:
    名称:
    Regioselective Trapping of Terminal Di-, Tri-, and Tetraynes with Benzyl Azide
    摘要:
    The reaction of benzyl azide with terminal di-, tri-, and tetraynes appended with a range of functional groups has been explored. Standard reaction conditions for BnN3 catalyzed by CuSO(4)(.)5H(2)O gave alkynyl, butadiynyl, and hexatriynyl triazoles in moderate to good yields. The reaction proceeds regioselectively as determined by the X-ray crystallographic analysis of three derivatives (1c, 1d, and 3c), and no evidence of multiple azide addition to the polyyne framework is observed.
    DOI:
    10.1021/ol062522a
  • 作为产物:
    描述:
    3-(三异丙硅基)丙炔醛正丁基锂 、 4 A molecular sieve 、 Celite 、 三苯基膦pyridinium chlorochromate 作用下, 以 四氢呋喃正己烷二氯甲烷甲苯 为溶剂, 反应 7.5h, 生成 Deca-1,3,5-triynyl-triisopropyl-silane
    参考文献:
    名称:
    Regioselective Trapping of Terminal Di-, Tri-, and Tetraynes with Benzyl Azide
    摘要:
    The reaction of benzyl azide with terminal di-, tri-, and tetraynes appended with a range of functional groups has been explored. Standard reaction conditions for BnN3 catalyzed by CuSO(4)(.)5H(2)O gave alkynyl, butadiynyl, and hexatriynyl triazoles in moderate to good yields. The reaction proceeds regioselectively as determined by the X-ray crystallographic analysis of three derivatives (1c, 1d, and 3c), and no evidence of multiple azide addition to the polyyne framework is observed.
    DOI:
    10.1021/ol062522a
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文献信息

  • Reactions of Terminal Polyynes with Benzyl Azide
    作者:Thanh Luu、Boris J. Medos、Erin R. Graham、Danielle M. Vallee、Robert McDonald、Michael J. Ferguson、Rik R. Tykwinski
    DOI:10.1021/jo101870y
    日期:2010.12.17
    Terminal di-, tri-, tetra-, and pentaynes substituted with a variety of functional groups react with benzyl azide in the presence of CuSO4 center dot 5H(2)O and ascorbic acid to give derivatives of 4-ethynyl-, 4-butadiynyl-, 4-hexatriynyl-, and 4-octatetraynyl-,2,3-triazoles in moderate to good yields. These reactions appear to proceed regioselectively, and functionalization occurs exclusively at the terminal alkyne moiety. As well, no evidence of multiple azide additions to the polyyne framework is observed. X-ray crystallographic analysis of nine derivatives is used to document the regioselectivity of the reaction as well as outline structural characteristics of the 1,2,3-triazole products.
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