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4,4'-bis(tricyclohexyltinmethyl)biphenyl | 740810-41-7

中文名称
——
中文别名
——
英文名称
4,4'-bis(tricyclohexyltinmethyl)biphenyl
英文别名
——
4,4'-bis(tricyclohexyltinmethyl)biphenyl化学式
CAS
740810-41-7
化学式
C50H78Sn2
mdl
——
分子量
916.589
InChiKey
MCEZXIKAIIUABT-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:
    811.0±75.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    16.42
  • 重原子数:
    52
  • 可旋转键数:
    11
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.76
  • 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:
    4,4'-bis(tricyclohexyltinmethyl)biphenyl四氯化锡甲苯 为溶剂, 以80%的产率得到4,4'-bis(trichlorotinmethyl)biphenyl
    参考文献:
    名称:
    α,ω-Bis(trialkynyltin) Compounds with a Linear or Cross-Shaped Spacer
    摘要:
    The preparation of arylene-, alkylene-, or dimethylenediphenyl-bridged bis(trichlorotin) compounds with two or three phenyl rings from the reaction of the corresponding hexacyclohexyl derivatives with tin tetrachloride is described. Hexachlorides with mixed aryl-alkyl bridges were prepared in the same way. When arylene-bridged ditins were substituted on aryl rings with alkoxy groups, it was necessary to use hexamethyl derivatives instead of the cyclohexyl compounds to obtain the corresponding hexachlorides. In these compounds, weak inter- and/or intramolecular interactions were detected by X-ray analysis. The ditin hexachlorides were transformed into the corresponding hexaalkynyl derivatives, precursors for hybrid materials.
    DOI:
    10.1021/om070078p
  • 作为产物:
    描述:
    联苯二氯苄三环己基氯化锡 在 magnesium 作用下, 以 四氢呋喃 为溶剂, 以80%的产率得到4,4'-bis(tricyclohexyltinmethyl)biphenyl
    参考文献:
    名称:
    α,ω-Bis(trialkynyltin) Compounds with a Linear or Cross-Shaped Spacer
    摘要:
    The preparation of arylene-, alkylene-, or dimethylenediphenyl-bridged bis(trichlorotin) compounds with two or three phenyl rings from the reaction of the corresponding hexacyclohexyl derivatives with tin tetrachloride is described. Hexachlorides with mixed aryl-alkyl bridges were prepared in the same way. When arylene-bridged ditins were substituted on aryl rings with alkoxy groups, it was necessary to use hexamethyl derivatives instead of the cyclohexyl compounds to obtain the corresponding hexachlorides. In these compounds, weak inter- and/or intramolecular interactions were detected by X-ray analysis. The ditin hexachlorides were transformed into the corresponding hexaalkynyl derivatives, precursors for hybrid materials.
    DOI:
    10.1021/om070078p
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文献信息

  • α,ω-Bis(trialkynyltin) Compounds with a Linear or Cross-Shaped Spacer
    作者:Hicham Elhamzaoui、Bernard Jousseaume、Thierry Toupance、Hassan Allouchi
    DOI:10.1021/om070078p
    日期:2007.7.30
    The preparation of arylene-, alkylene-, or dimethylenediphenyl-bridged bis(trichlorotin) compounds with two or three phenyl rings from the reaction of the corresponding hexacyclohexyl derivatives with tin tetrachloride is described. Hexachlorides with mixed aryl-alkyl bridges were prepared in the same way. When arylene-bridged ditins were substituted on aryl rings with alkoxy groups, it was necessary to use hexamethyl derivatives instead of the cyclohexyl compounds to obtain the corresponding hexachlorides. In these compounds, weak inter- and/or intramolecular interactions were detected by X-ray analysis. The ditin hexachlorides were transformed into the corresponding hexaalkynyl derivatives, precursors for hybrid materials.
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同类化合物

邻苯二甲酰基 邻甲基二苯甲酮自由基阳离子 [6]轴烯 7,7,8,8-四氰基对苯二醌二甲烷 7,7,8,8-四氰基喹啉二甲烷 四硫富瓦烯盐 5,6-二亚甲基环己-1,3-二烯 2-氟-7,7,8,8-四氰喹啉并二甲烷 2-[4-[[4-[二(2-羟基乙基)氨基]苯基]-氰基亚甲基]-2,3,5,6-四氟环己-2,5-二烯-1-亚基]丙二腈 2,5-二甲基-7,7,8,8-四氰醌二甲烷 2,5-二氟-7,7,8,8-四氰基苯醌二甲烷 2,3,5,6-四氟-7,7',8,8'-四氰二甲基对苯醌 (1Z)-2-氯-1-(3-甲基-6-亚甲基-2,4-环己二烯-1-亚基)乙醇 (1E)-1-(6-亚甲基-2,4-环己二烯-1-亚基)乙醇 3,6-bis(1,3-dithiolan-2-ylidene)-1,2,4,5-cyclohexanetetrone Sodium;2-[4-(dicyanomethylidene)cyclohexa-2,5-dien-1-ylidene]propanedinitrile 2-pentadecyl-7,7,8,8-tetracyanoquinodimethane α,α'-bis(tributylstannyl)-o-xylene Li{(NC)2CC6H4C(CN)2-p} 7,7,8-tricyano-8-(1-piperidinyl)quinodimethane methyl 4-(1-diazo-2,2,2-trifluoroethyl)benzoate 1,4-Cyclohexadiene, 1,4-dimethyl-3,6-bis(methylene)- p-Chinobis(benzo-1,3-dithiol) 3,4-dimethylenebicyclo[4.2.0]octa-1,5-diene 1,2,4,5-tetramethylenebenzene 7-(p-Aminophenyl)-7,8,8-tricyanochinodimethid tetracyanodiphenoquinodimethane bis<1,2,5>selenadiazolotetracyanoquinodimethan 4,8-bis(1,3-dithiol-2-ylidene)-4H,8H-benzo<1,2-c:4,5-c'>bis<1,2,5>selenadiazole 2-(4-dicyanomethylenecyclohexa-2,5-dienylidene)imidazolidine [1-{[4-(dicyanomethylene)cyclohexa-2,5-dien-1-ylidene][4-(dimethylamino)phenyl]-methyl}-3-(trimethylsilyl)prop-2-yn-1-ylidene]malononitrile (4-{2-butyl-3,3-dicyano-1-[4-(dimethylamino)phenyl]prop-2-en-1-ylidene}cyclohexa-2,5-dien-1-ylidene)malononitrile (4-{2-(dicyanomethylene)-1,4-bis[4-(dimethylamino)phenyl]but-3-yn-1-ylidene}-cyclohexa-2,5-dien-1-ylidene)malononitrile 2-dodecyl-7,7,8,8-tetracyanoquinodimethane 3,6--1,4-cyclohexadien 4,4'-bis(4,4,5,5-tetramethyl-1-yloxy-3-oxidoimidazolin-2-yl)phenyldiazomethane Hexa-propyliden-cyclohexan α-methyl-p-xylylene o-dimethylquinodimethane 3,5-Bismethylen-4-vinyl-1-cyclohexen Cyclohexane, hexaethylidene- [4-(4,4,5,5-tetramethyl-1-yloxy-3-oxidoimidazolin-2-yl)phenyl]phenyldiazomethane (5E,6E)-5,6-bis(bromomethylidene)cyclohexa-1,3-diene 2-octadecyl-7,7,8,8-tetracyanoquinodimethane 2,2-diphenyl-2-stanna-indane chloro-tetracyanoquinodimethane 2-Brom-5-methyl-7,7,8,8-tetracyanochinodimethan 2-bromo-7,7,8,8-tetracyanoquinodimethane α,α,α',α'-tetrafluoro-p-xylylene di(2,6-dimethyl-4-cyanophenyl)carbene