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[benzene-1,3,5-triyltris(methylene)]tris(triphenylphosphonium) tribromide | 54771-95-8

中文名称
——
中文别名
——
英文名称
[benzene-1,3,5-triyltris(methylene)]tris(triphenylphosphonium) tribromide
英文别名
benzene-1,3,5-triyltris(methylene)tris(triphenylphosphonium) bromide;1,3,5-(tris-[(triphenylphosphonio)methyl])-benzene tribromide;1,3,5-tris((triphenylphosphonium)methyl)benzene tribromide;[1,3,5-tris(triphenylphosphoniomethyl)benzene] tribromide;1,3,5-tris-(triphenylphosphonio-methyl)-benzene; tris bromide;1,3,5-Tris-(triphenylphosphonio-methyl)-benzol; Tris-bromid
[benzene-1,3,5-triyltris(methylene)]tris(triphenylphosphonium) tribromide化学式
CAS
54771-95-8
化学式
3Br*C63H54P3
mdl
——
分子量
1143.76
InChiKey
CVTOOZSGJQGAPL-UHFFFAOYSA-M
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):
    9.17
  • 重原子数:
    67.0
  • 可旋转键数:
    15.0
  • 环数:
    10.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    0.0

SDS

SDS:5d517165a43815bb60ae37d1cee670c8
查看

反应信息

  • 作为反应物:
    描述:
    [benzene-1,3,5-triyltris(methylene)]tris(triphenylphosphonium) tribromidepotassium tert-butylate三溴化硼 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 38.0h, 生成 (E,E,E)-1,3,5-tris[4-(acetylthio)styryl]benzene
    参考文献:
    名称:
    Novel Synthesis of Protected Thiol End-Capped Stilbenes and Oligo(phenylenevinylene)s (OPVs)
    摘要:
    The first general procedures for preparation of thiol end-capped stilbenes and oligo(phenylene-vinylene)s (OPVs) with tert-butyl- and acetyl-protected thiol termini have been developed. These reactions proceed via Br/Li exchange, McMurry, and Wittig-type reactions. The thiol functionality is protected against strong basic and acidic reaction conditions as a t-Bu sulfide. As a key point in the method, reprotection of the thiol group is accomplished by means of acetyl chloride and boron tribromide. The novel strategy forms the basis for stepwise introduction of 4-mercaptostyryl units in OPVs. The new mono-, di-, and trimercapto OPVs have potential applications as one, two, and three terminal molecular devices in gold nanoparticle clusters, self-assembled monolayers, and optoelectronic devices.
    DOI:
    10.1021/jo0263770
  • 作为产物:
    参考文献:
    名称:
    New planar and soluble tris-tetrathiafulvalene derivatives with threefold-symmetry
    摘要:
    Novel trimeric tetrathiafulvalene (TTF) derivatives with threefold-symmetry are built on the 1,3,5