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1,8-dimethylthianthrene | 1207270-57-2

中文名称
——
中文别名
——
英文名称
1,8-dimethylthianthrene
英文别名
——
1,8-dimethylthianthrene化学式
CAS
1207270-57-2
化学式
C14H12S2
mdl
——
分子量
244.381
InChiKey
FGLZRXLEFOFUTL-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):
    4.9
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    50.6
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    5-甲基-1,3-苯并二硫醇-2-亚胺 、 3-methyl-2-(trimethylsilyl)phenyl trifluoromethanesulfonate 在 potassium fluoride 、 18-冠醚-6 作用下, 以 乙腈 为溶剂, 反应 16.0h, 生成 1,8-dimethylthianthrene1,7-dimethylthianthrene
    参考文献:
    名称:
    利用两亲性:易于金属与噻吩和相关硫杂环的接触
    摘要:
    使易获得的苯并二硫代亚亚甲基与被吸电子基团取代的芳烃或炔烃反应,得到相应的噻吩并蒽或苯并[b] [1,4]二硫氨酸衍生物。该转化在温和的反应条件下进行,而无需...
    DOI:
    10.1039/c5cc01757b
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文献信息

  • Oxidative Coupling of Diaryldisulfides by MoCl<sub>5</sub>to Thianthrenes
    作者:Anke Spurg、Gregor Schnakenburg、Siegfried R. Waldvogel
    DOI:10.1002/chem.200902466
    日期:2009.12.14
    Oxidative CS coupling: The oxidative coupling reaction of 1,2‐diaryldisulfides by using MoCl5 or mixtures thereof with TiCl4 gives fast and efficient access to dibenzo[b,e] [1,4]‐dithiins such as that depicted (thianthrenes).
    氧化Ç 小号耦合:通过使用代替MoCl 1,2- diaryldisulfides氧化偶联反应5或它们的混合物用TiCl 4 4给出了快速和高效地访问二苯并[ b,ë ] [1,4] -dithiins如所描绘的(蒽)。
  • Organic electroluminescence device
    申请人:UDC Ireland
    公开号:US10454042B2
    公开(公告)日:2019-10-22
    An object of the present invention is to provide an organic electroluminescence device having excellent light emission efficiency and durability, in particular, durability when driving at a high temperature. Provided is an organic electroluminescence device including on a substrate a pair of electrodes, and at least one layer of an organic layer including a light emitting layer containing a light emitting material disposed between the electrodes, wherein the light emitting layer includes at least each one of specific indolocarbazole derivatives and specific condensed ring metal complexes.
    本发明的目的是提供一种有机电致发光器件,该器件具有优异的发光效率和耐用性,特别是在高温驱动时的耐用性。本发明提供了一种有机电致发光器件,包括在基底上的一对电极,以及至少一层有机层,该有机层包括设置在电极之间的包含发光材料的发光层,其中发光层包括特定吲哚咔唑衍生物和特定缩合环金属配合物中的至少一种。
  • COMPOUND FOR ORGANIC ELECTROLUMINESCENT ELEMENT AND ORGANIC ELECTROLUMINESCENT ELEMENT
    申请人:Nippon Steel Chemical Co., Ltd.
    公开号:EP1956022B1
    公开(公告)日:2012-07-25
  • Compound for Use in Organic Electroluminescent Device and Organic Electroluminescent Device
    申请人:Komori Masaki
    公开号:US20090302742A1
    公开(公告)日:2009-12-10
    Disclosed are an organic electroluminescent device (organic EL device) which is improved in luminous efficiency, fully secured of driving stability, and simple in constitution and a compound for use therein. The organic electroluminescent device comprises a light-emitting layer disposed between an anode and a cathode piled one upon another on a substrate and the light-emitting layer contains a phosphorescent dopant and a compound for use in an organic electroluminescent device having two or more indolocarbazole skeletons as a host material. An example of the compound having indolocarbazole skeletons for use in the device is expressed by the following formula.
  • COMPOUND FOR ORGANIC OPTOELECTRONIC DEVICE, ORGANIC LIGHT EMITTING DIODE INCLUDING THE SAME, AND DISPLAY DEVICE INCLUDING THE ORGANIC LIGHT EMITTING DIODE
    申请人:JUNG Sung-Hyun
    公开号:US20120091445A1
    公开(公告)日:2012-04-19
    A compound for an organic optoelectronic device, an organic light emitting diode, and a display device, the compound including substituents represented by the following Chemical Formulae 1 and 2:
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同类化合物

硅烷,1,9-硫杂蒽二基二[三甲基- 甲硫芬 噻蒽-2-硼酸 噻蒽-1,9-二甲酸 噻蒽 5-氧化物 噻蒽 5,10-二氧化物 噻蒽 噻吩-1-羧酸 噻吩-1-硼酸 六氟磷酸1-氯-5-苯基-硫杂蒽-5-正离子 二甲基噻蒽 2-溴噻蒽 2-吗啉-4-基-6-噻蒽-1-基吡喃-4-酮 2,7-噻蒽二甲酸 2,7-二氟噻蒽 2,7-二乙酰基噻蒽 2,3,7,8-四甲基-1,4,6,9-噻蒽四酮 2,3,7,8-四氯噻蒽 1,4,6,9-噻蒽四酮 2,7-bis(9-carbazolyl)thianthrene 1,7-dimethylthianthrene 13,13,14,14-Tetracyano-2-methylbenzonaphtho<2,3-e><1,4>dithiin-6,11-quinodimethane 2-methyl-5,12-dithianaphthacene 13,13,14,14-Tetracyanobenzonaphtho<2,3-e><1,4>dithiin-6,11-quinodimethane 2,5-dihexylbenzo[5,6][1,4]dithiino[2,3-e]pyrrolo[3,4-g]isoindole-1,3,4,6(2H,5H)-tetraone 2-cyanothianthrene 1-cyanothianthrene 2,3-difluorothianthrene 3-(1-thianthrenyl)phenol 2,7-diisopropylthianthrene-5,5,10,10-tetraoxide (Z)-2-(5-thianthreniumyl)-2-hexene perchlorate (E)-2-(5-thianthreniumyl)-2-hexene perchlorate (Z)-3-(5-thianthreniumyl)-2-hexene perchlorate (E)-3-(5-thianthreniumyl)-2-hexene perchlorate Phenylthianthren-2-ylmethanol 1,1′-methylenedithianthrene 1,1′-(chloromethylene)dithianthrene 1,6-dithianthren-1-ylhexane-1,6-diol 9-(4-methylacetophenone)thianthrenium perchlorate Thianthren-1-ylphenylmethanol Diphenylthianthren-1-ylmethanol 4,4,5,5-tetramethyl-2-(thianthren-2-yl)-1,3,2-dioxaborolane thianthrene-2-sulfonic acid 2-(thianthren-1-ylsulfanyl)pyridine 2,8-dibromothianthrene dithianthren-1-ylmethanol 5-(2-acetamido-4,5-dimethylphenyl)thianthreniumyl perchlorate 5-(4-anisyl)thianthreniumyl perchlorate 1-tributylstannylthianthrene 5-(3-bromo-4-methoxyphenyl)thianthreniumyl perchlorate