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2,3-dibromo-6,13-bis(diphenylmethylene)-9,10-bis(dodecyloxy)-6,13-dihydropentacene | 1154754-80-9

中文名称
——
中文别名
——
英文名称
2,3-dibromo-6,13-bis(diphenylmethylene)-9,10-bis(dodecyloxy)-6,13-dihydropentacene
英文别名
6,13-Dibenzhydrylidene-2,3-dibromo-9,10-didodecoxypentacene
2,3-dibromo-6,13-bis(diphenylmethylene)-9,10-bis(dodecyloxy)-6,13-dihydropentacene化学式
CAS
1154754-80-9
化学式
C72H78Br2O2
mdl
——
分子量
1135.22
InChiKey
GHSFBPDLSCAYTN-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):
    25.8
  • 重原子数:
    76
  • 可旋转键数:
    28
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2,3-dibromo-6,13-bis(diphenylmethylene)-9,10-bis(dodecyloxy)-6,13-dihydropentacene 在 iron(III) chloride 作用下, 以 硝基甲烷二氯甲烷 为溶剂, 反应 0.58h, 以79%的产率得到16,17-dibromo-6,7-bis(dodecyloxy)-13,20-diphenylnaphtho[1,2,3,4-fgh]trinaphthylene
    参考文献:
    名称:
    Expeditious Synthesis of Contorted Hexabenzocoronenes
    摘要:
    Contorted hexabenzocoronenes (HBCs) have been synthesized in an expedited manner utilizing a double Barton-Kellogg olefination reaction and a subsequent Scholl cyclization. The scope of both transformations was investigated using a series of pentacene quinones and double olefin precursors. The utility,of these reactions to help create functionalized and oligomeric HBCs in a rapid manner is demonstrated.
    DOI:
    10.1021/ol9001834
  • 作为产物:
    描述:
    2',3'-dibromo-9',10'-bis(dodecyloxy)-3,3,3'',3''-tetraphenyldispiro[thiirane-2,6'-pentacene-13',2''-thiirane]三苯基膦 作用下, 以 对二甲苯 为溶剂, 反应 16.0h, 以97%的产率得到2,3-dibromo-6,13-bis(diphenylmethylene)-9,10-bis(dodecyloxy)-6,13-dihydropentacene
    参考文献:
    名称:
    Expeditious Synthesis of Contorted Hexabenzocoronenes
    摘要:
    Contorted hexabenzocoronenes (HBCs) have been synthesized in an expedited manner utilizing a double Barton-Kellogg olefination reaction and a subsequent Scholl cyclization. The scope of both transformations was investigated using a series of pentacene quinones and double olefin precursors. The utility,of these reactions to help create functionalized and oligomeric HBCs in a rapid manner is demonstrated.
    DOI:
    10.1021/ol9001834
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同类化合物

并六苯 并五苯 十四氟并五苯 二苯并[去,St]并五苯 二苯并[hi,wx]庚省 二苯并[fg,qr]戊省 二苯并[a,l]并五苯 二苯并[a,c]戊省 7,14-二苯并五苯 6,13-双(三甲硅基乙炔基)并五苯 6,13-双(三异丙基甲硅烷基乙炔基)并五苯 6,13-双(2-噻吩基)并五苯 6,13-二氯并五苯 2,3,9,10-四(4-叔丁基苯基)并五苯 1,4,8,11-戊省四酮,6,13-二己基-2,3,9,10-四甲基- 5-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl]-14-phenylpentacene 5-(4-decyloxy-phenyl)-14-phenyl-pentacene 1,2,3,4,9,10-Hexaphenyl-anthracene 1,4-bis(trimethylsilyl)-2,3-dimethylnaphthacene 6,6’-bipentacene Tri(propan-2-yl)-[2-[7,14,24,31-tetraphenyl-19-[2-tri(propan-2-yl)silylethynyl]-2-nonacyclo[18.14.0.03,18.05,16.06,15.08,13.022,33.023,32.025,30]tetratriaconta-1,3,5(16),6,8,10,12,14,17,19,21,23,25,27,29,31,33-heptadecaenyl]ethynyl]silane Tri(propan-2-yl)-[2-[7,18,28,39-tetraphenyl-23-[2-tri(propan-2-yl)silylethynyl]-2-undecacyclo[22.18.0.03,22.05,20.06,19.08,17.010,15.026,41.027,40.029,38.031,36]dotetraconta-1,3,5(20),6,8,10,12,14,16,18,21,23,25,27,29,31,33,35,37,39,41-henicosaenyl]ethynyl]silane 6,13-bis(triisobutylsilylethynyl)pentacene 1,4-Bis(2,2-dimethylpropoxy)anthracene 2,3-dibromo-6,13-bis(diphenylmethylene)-9,10-bis(dodecyloxy)-6,13-dihydropentacene dimethyl-2,3 diacetoxy-1,4 naphtacene 2,9-didecylpentacene 2,9-diundecylpentacene 2,9-dioctylpentacene 7-Ethyl-heptaphen 2,9-dibutylpentacene 8,9,10-Trichlorocyclohept-s-indacen 2,9-dipentylpentacene 2,3-bis(hexadecyloxy)-5,12-diphenyltetracene naphthacene; compound with antimony (V)-chloride 6,13-bis[4-(trimethylsilylethynyl)phenyl]pentacene 2,8-di(2-(trimethylsilyl)ethylthio)tetracene 2,8-di(acetylthio)tetracene 6,13-bis(cyclopropyldiisopropylsilylethynyl)pentacene naphthacene-5,6-diol 2-(2-(trimethylsilyl)ethylthio)tetracene 6,7,14,15,22,23-Hexamethoxyanthra<2,3-j>heptaphen 2,9-diheptylpentacene 5,14-diphenyl-7,12-bis(2-(triethylsilyl)ethyl)pentacene 5,8-difluorobenzophenanthrene 6,13-bis((1-methylenepropyl)diisopropylsilylethynyl)pentacene