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1,3,5-tris(chlorodimethylsilyl)benzene | 120666-38-8

中文名称
——
中文别名
——
英文名称
1,3,5-tris(chlorodimethylsilyl)benzene
英文别名
Silane, 1,3,5-benzenetriyltris[chlorodimethyl-;[3,5-bis[chloro(dimethyl)silyl]phenyl]-chloro-dimethylsilane
1,3,5-tris(chlorodimethylsilyl)benzene化学式
CAS
120666-38-8
化学式
C12H21Cl3Si3
mdl
——
分子量
355.914
InChiKey
LBFOVAINRVHXRL-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):
    3.64
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    1,3,5-tris(chlorodimethylsilyl)benzene18-冠醚-6sodium 作用下, 以 甲苯 为溶剂, 以0.22%的产率得到4,4,5,5,11,11,12,12,15,15,16,16-dodecamethyl-4,5,11,12,15,16-hexasilatetracyclo[6.6.2.13,13.16,10]octadeca-1(14),2,6,8,10(18),13(17)-hexaene
    参考文献:
    名称:
    Sekiguchi, Akira; Yatabe, Tetsuo; Kabuto, Chizuko, Angewandte Chemie, 1989, vol. 101, # 6, p. 778 - 780
    摘要:
    DOI:
  • 作为产物:
    描述:
    1,3,5-三溴苯magnesium 作用下, 以 四氢呋喃 为溶剂, 反应 43.0h, 生成 1,3,5-tris(chlorodimethylsilyl)benzene
    参考文献:
    名称:
    Siloxa-bridged-cyclophanes featuring benzene, thiophene and pyridine units
    摘要:
    通过水解氯硅烷单体,制备了两个八甲基二硅氧烷键合的[3.3]环烷(1 和 2)和一个十二甲基三硅氧烷键合的[3.3.3]笼状化合物(3)。此外,还采用这种一般方法制备了两种具有两个噻吩(14)或吡啶(17)分子的八甲基二硅氧烷键合[3.3]杂环化合物。
    DOI:
    10.1039/b211045h
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文献信息

  • A sandwich-shaped M<sub>3</sub>L<sub>2</sub> zinc(<scp>ii</scp>) complex containing 1,3,5-tris(dimethyl(pyridin-3-yl)silyl)benzene: selective photoluminescence recognition of diiodomethane
    作者:Sangseok Lee、Haeri Lee、Ok-Sang Jung
    DOI:10.1039/c7dt01138e
    日期:——

    The selective small molecular recognition of a discrete sandwich-shaped M3L2 zinc(ii) complex showing strong blue photoluminescence has been investigated.

    翻译结果:

    研究了一种选择性小分子识别的离散三明治形状的M3L2ii)配合物,该配合物表现出强烈的蓝色光致发光。

  • Nanosized starlike molecules. Synthesis and optical properties of tris- and tetrakis[oligo(disilanylenebithienylene)dimethylsilyl]benzene
    作者:Akinobu Naka、Yoshiaki Matsumoto、Tatsuya Itano、Kei Hasegawa、Tomoaki Shimamura、Joji Ohshita、Atsutaka Kunai、Takae Takeuchi、Mitsuo Ishikawa
    DOI:10.1016/j.jorganchem.2008.10.053
    日期:2009.2
    The syntheses of two types of starlike molecules with the arms that extend to three and four directions have been reported. The molecules with the arms consisting of a regular alternating arrangement of a silicon-silicon bond and bithienylene unit that extend to three directions were synthesized by the reactions of 1,3,5-tris(chlorodimethylsilyl) benzene, which was chosen as a core, with the lithio[oligo(disilanylenebithienylene)] derivatives. The starlike molecules with extended arms to four directions were prepared by the reaction of 1,2,4,5-tetrakis(fluorodimethylsilyl) benzene used as a core, with lithio[oligo(disilanylenebithienylene)]s. UV-Vis absorption and fluorescence properties of these starlike molecules have been investigated in a dioxane solution. The present molecules showed absorption maxima in a range of 321-337 nm, and revealed higher fluorescence quantum yields than that of the corresponding linear polymer, poly[(tetraethyldisilanylene) bithiophene]. (C) 2008 Elsevier B.V. All rights reserved.
  • Polycylopentadienyls: Synthesis of arylsilylcyclopentadienyl compounds and their η5-complexes with tungsten
    作者:Herbert Plenio
    DOI:10.1016/0022-328x(92)83456-r
    日期:1992.2
    A general route to arylsilylcyclopentadienyl compounds starting from 1,4-C6H4Br2, 2,6-C5NH3Br2 and 1,3,5-C6H3Br3 is described. The aryl bromides were treated with Mg/ClSiMe2H to give the aryldimethylsilanes 1,4-C6H4(SiMe2H)2, 2,6-C5NH3(SiMe2H)2, and 1,3,5-C6H3(SiMe2H)3 which after reaction with Cl2 or Br2 yielded the aryldimethylsilyl halides 1,4-C6H4(SiMe2Br)2, 2,6-C5NH3 (SiMe2Br)2, 1,3,5-C6H3(SiMe2X)3 (X = Br or Cl) in excellent yields. The halide can be replaced by various cyclopentadienides to give aryldimethylsilylcyclopentadienes of the general type 1,4-C6H4 (SiMe2CP)2 and 1,3,5-C6H3(SiMe2CP)3 (Cp = C5H5 (8,11), C5H3(t-C4H9)2 (9,12), C5HMe4 (10,13)). Compounds C6H5(SiMe2(C5H5)), 1,4-C6H4(SiMe2(C5H5))2 (8) and 1,3,5-C6H3(SiMe2(C5H5))3 (11) were in turn treated with NaH, (MeCN)3W(CO)3, and MeI to give the eta-5-bound complexes C6H5 (SiMe2(C5H4)W(CO)3Me) (14), 1,4-C6H4(SiMe2(C5H4)W(CO)3Me)2 (15), 1,3,5-C6H3(SiMe2(C5H4)-W(CO)3Me)3 (16), which contain up to three half-sandwich units within one molecule.
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同类化合物

(2-溴乙氧基)-特丁基二甲基硅烷 鲸蜡基聚二甲基硅氧烷 骨化醇杂质DCP 马沙骨化醇中间体 马来酸双(三甲硅烷)酯 顺式-二氯二(二甲基硒醚)铂(II) 顺-N-(1-(2-乙氧基乙基)-3-甲基-4-哌啶基)-N-苯基苯酰胺 降钙素杂质13 降冰片烯基乙基三甲氧基硅烷 降冰片烯基乙基-POSS 间-氨基苯基三甲氧基硅烷 镓,二(1,1-二甲基乙基)甲基- 镁,氯[[二甲基(1-甲基乙氧基)甲硅烷基]甲基]- 锑,二溴三丁基- 铷,[三(三甲基甲硅烷基)甲基]- 铂(0)-1,3-二乙烯-1,1,3,3-四甲基二硅氧烷 钾(4-{[二甲基(2-甲基-2-丙基)硅烷基]氧基}-1-丁炔-1-基)(三氟)硼酸酯(1-) 金刚烷基乙基三氯硅烷 酰氧基丙基双封头 达格列净杂质 辛醛,8-[[(1,1-二甲基乙基)二甲基甲硅烷基]氧代]- 辛甲基-1,4-二氧杂-2,3,5,6-四硅杂环己烷 辛基铵甲烷砷酸盐 辛基衍生化硅胶(C8)ZORBAX?LP100/40C8 辛基硅三醇 辛基甲基二乙氧基硅烷 辛基三甲氧基硅烷 辛基三氯硅烷 辛基(三苯基)硅烷 辛乙基三硅氧烷 路易氏剂-3 路易氏剂-2 路易士剂 试剂Cyanomethyl[3-(trimethoxysilyl)propyl]trithiocarbonate 试剂3-[Tris(trimethylsiloxy)silyl]propylvinylcarbamate 试剂3-(Trimethoxysilyl)propylvinylcarbamate 试剂2-(Trimethylsilyl)cyclopent-2-en-1-one 试剂11-Azidoundecyltriethoxysilane 西甲硅油杂质14 衣康酸二(三甲基硅基)酯 苯胺,4-[2-(三乙氧基甲硅烷基)乙基]- 苯磺酸,羟基-,盐,单钠聚合甲醛,1,3,5-三嗪-2,4,6-三胺和脲 苯甲醇,a-[(三苯代甲硅烷基)甲基]- 苯并磷杂硅杂英,5,10-二氢-10,10-二甲基-5-苯基- 苯基二甲基氯硅烷 苯基二甲基乙氧基硅 苯基二甲基(2'-甲氧基乙氧基)硅烷 苯基乙酰氧基三甲基硅烷 苯基三辛基硅烷 苯基三甲氧基硅烷