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1,5,1',5'-tetraphenyl-[3,3']bicyclohexa-1,4-dienylidene-6,6'-dione | 3550-01-4

中文名称
——
中文别名
——
英文名称
1,5,1',5'-tetraphenyl-[3,3']bicyclohexa-1,4-dienylidene-6,6'-dione
英文别名
1,5,1',5'-Tetraphenyl-[3,3']bicyclohexa-1,4-dienyliden-6,6'-dion;3,3',5,5'-Tetraphenyl-4,4'-biphenylquinone;4-(4-oxo-3,5-diphenylcyclohexa-2,5-dien-1-ylidene)-2,6-diphenylcyclohexa-2,5-dien-1-one
1,5,1',5'-tetraphenyl-[3,3']bicyclohexa-1,4-dienylidene-6,6'-dione化学式
CAS
3550-01-4
化学式
C36H24O2
mdl
——
分子量
488.585
InChiKey
MOHKIBLECXHJQD-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

  • 熔点:
    270 °C
  • 沸点:
    754.1±60.0 °C(Predicted)
  • 密度:
    1.250±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.7
  • 重原子数:
    38
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:ae5322b3eaa516f2ecf8f0e092b6bce3
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反应信息

  • 作为反应物:
    描述:
    1,5,1',5'-tetraphenyl-[3,3']bicyclohexa-1,4-dienylidene-6,6'-dione溶剂黄146 作用下, 以 甲苯 为溶剂, 生成 4,4'-Dimethoxy-3,3',5,5'-tetraphenylbiphenyl
    参考文献:
    名称:
    Hageman,H.J.; Huysmans,W.G.B., Recueil des Travaux Chimiques des Pays-Bas, 1972, vol. 91, p. 528 - 532
    摘要:
    DOI:
  • 作为产物:
    描述:
    2,6-二苯基苯酚高氯酸cerium(III) perchlorate 、 cerium(IV) perchlorate 作用下, 以 溶剂黄146乙腈 为溶剂, 以70%的产率得到1,5,1',5'-tetraphenyl-[3,3']bicyclohexa-1,4-dienylidene-6,6'-dione
    参考文献:
    名称:
    Oxidative Coupling of Some 2,6-Disubstituted Phenol Derivatives in Perchloric Acid Mediated by Cerium(IV) Ions
    摘要:
    DOI:
    10.1007/pl00013485
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文献信息

  • HETEROCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE
    申请人:Ohrui Hiroki
    公开号:US20080138656A1
    公开(公告)日:2008-06-12
    Provided is a novel heterocyclic compound which is useful as a material for an organic electroluminescent device. The heterocyclic compound is represented by the general formula [I]: wherein X represents a nitrogen atom or a carbon atom; Y represents O or S; R 1 and R 2 each represent, independently of one another, a group selected from the group consisting of a substituted or unsubstituted alkyl group and the like; a represents 0 or more and 3 or less; b represents 0 or more and 3 or less; and Ar 1 represents a substituted or unsubstituted heterocyclic ring or the like; and n represents an integer of 2 to 10.
    提供了一种新颖的杂环化合物,可用作有机电致发光器件的材料。这种杂环化合物由通用公式[I]表示:其中X代表氮原子或碳原子;Y代表O或S;R1和R2分别独立地代表从取代或未取代的烷基等组成的组;a表示0或更多,但不超过3;b表示0或更多,但不超过3;Ar1代表取代或未取代的杂环环或类似物;n表示2到10之间的整数。
  • PYRENE COMPOUND AND ORGANIC LIGHT EMITTING DEVICE
    申请人:Suzuki Koichi
    公开号:US20080119671A1
    公开(公告)日:2008-05-22
    An object of the present invention is to provide a novel pyrene compound. Provided is a pyrene compound represented by the following general formula (I): wherein: R 1 and R 2 each represent a substituted or unsubstituted alkyl group; and Ar 1 , Ar 2 , Ar 3 , and Ar 4 each represent a substituted or unsubstituted aryl group and the like.
    本发明的目的是提供一种新型的芘化合物。提供的是一种由以下通式(I)表示的芘化合物: 其中:R1和R2各代表取代或未取代的烷基;Ar1、Ar2、Ar3和Ar4各代表取代或未取代的芳基等。
  • CARBAZOLE DERIVATIVE AND ORGANIC LIGHT EMITTING DEVICE USING THE SAME
    申请人:Igawa Satoshi
    公开号:US20080131731A1
    公开(公告)日:2008-06-05
    Provided is an organic light emitting device including: a pair of electrodes including an anode and a cathode; and at least one layer formed of an organic compound interposed between the pair of electrodes, in which the at least one layer formed of the organic compound layer contains at least one kind of the carbazole derivative represented by the following general formula (I). The organic light emitting device has an optical output with extremely high efficiency and a high luminance and has an extremely high durability.
    提供的是一种有机发光装置,包括:一对电极,包括阳极和阴极;以及至少一层有机化合物层,夹在一对电极之间,其中所述至少一层有机化合物层包含至少一种由以下通式(I)表示的咔唑衍生物。该有机发光装置具有极高的光学输出效率和高亮度,并具有极高的耐久性。
  • Nitrations and oxidations with inorganic nitrate salts in trifluoroacetic anhydride
    作者:J. V. Crivello
    DOI:10.1021/jo00328a013
    日期:1981.7
  • Oxidation of 2,6-disubstituted phenols as a route to 3,5,3?,5?-tetrasubstituted diphenoquinones and 4,4?-dihydroxydiphenyls
    作者:M. Sh. Vakhitova、B. I. Pantukh、G. A. Tolstikov、O. P. Yablonskii、R. B. Svitych
    DOI:10.1007/bf00960131
    日期:1987.8
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