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4-(tert-butyldimethylsilanyloxymethyl)-1-(3-(2-(5-chloro-2-methylthiophen-3-yl)cyclopent-1-enyl)-2-methylbenzo[b]thiophen-5-yl)piperidine | 1351277-26-3

中文名称
——
中文别名
——
英文名称
4-(tert-butyldimethylsilanyloxymethyl)-1-(3-(2-(5-chloro-2-methylthiophen-3-yl)cyclopent-1-enyl)-2-methylbenzo[b]thiophen-5-yl)piperidine
英文别名
Tert-butyl-[[1-[3-[2-(5-chloro-2-methylthiophen-3-yl)cyclopenten-1-yl]-2-methyl-1-benzothiophen-5-yl]piperidin-4-yl]methoxy]-dimethylsilane
4-(tert-butyldimethylsilanyloxymethyl)-1-(3-(2-(5-chloro-2-methylthiophen-3-yl)cyclopent-1-enyl)-2-methylbenzo[b]thiophen-5-yl)piperidine化学式
CAS
1351277-26-3
化学式
C31H42ClNOS2Si
mdl
——
分子量
572.351
InChiKey
ONSTXGIQTOETPP-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):
    10.57
  • 重原子数:
    37
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    69
  • 氢给体数:
    0
  • 氢受体数:
    4

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

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文献信息

  • Synthesis and Characterization of Nonsymmetric Cyclopentene-Based Dithienylethenes
    作者:Vasily A. Migulin、Michael M. Krayushkin、Valery A. Barachevsky、Olga I. Kobeleva、Tatyana M. Valova、Konstantin A. Lyssenko
    DOI:10.1021/jo201966g
    日期:2012.1.6
    Nonsymmetric cyclopentene-based dithienylethenes, containing both thienyl and benzothienyl units, have been synthesized for the first time, employing intramolecular McMurry reaction as a key transformation to target compounds 10 and 16. Photochromic properties of these compounds were examined in toluene and acetonitrile solutions, PMMA layers, solid films, and crystal phase. To explain an unprecedented single-crystalline photochromism phenomena of 10, X-ray crystallographic analysis was performed, revealing a significant influence of strong S center dot center dot center dot S interatomic interactions on the intramolecular distance between two photochemical reaction centers in the molecule. Compound 16 could be further synthetically modified in a step-by-step manner, thus serving as potential key intermediate to various complex bifunctional photochromic molecules.
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