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10-Imidazol-1-yldecoxy(triphenyl)silane | 1234388-35-2

中文名称
——
中文别名
——
英文名称
10-Imidazol-1-yldecoxy(triphenyl)silane
英文别名
10-imidazol-1-yldecoxy(triphenyl)silane
10-Imidazol-1-yldecoxy(triphenyl)silane化学式
CAS
1234388-35-2
化学式
C31H38N2OSi
mdl
——
分子量
482.741
InChiKey
DULADYNVXNESQH-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):
    5.69
  • 重原子数:
    35
  • 可旋转键数:
    15
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    27
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    三苯基氯硅烷1-(10-羟基癸)咪唑吡啶 作用下, 以 乙腈 为溶剂, 以45%的产率得到10-Imidazol-1-yldecoxy(triphenyl)silane
    参考文献:
    名称:
    Synthesis and characterization of imidazole–triphenylsilane complexes
    摘要:
    Three imidazole-based triphenylsilane complexes were synthesized as preliminary model complexes to those that have been proposed as intermediates during the enzymatic biomineralization of silica by certain sponges. The active site of the enzyme includes histidine-serine moieties that appear to be vital to functionality. The model compounds include ligands that are bound to the silicon via a Si-O-C linkage and have a potentially chelating imidazole ring. Synthesis of these compounds was achieved by reaction of triphenylchlorosilane with two equivalents of ligand, one equivalent acting as a base for the HCl generated during the reaction. The compounds are highly reactive toward hydrolysis and were characterized by NMR, MS, elemental analysis, and X-ray crystallography. (C) 2010 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2010.03.005
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