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1-bromo-thianthrene | 94522-76-6

中文名称
——
中文别名
——
英文名称
1-bromo-thianthrene
英文别名
1-Bromothianthrene
1-bromo-thianthrene化学式
CAS
94522-76-6
化学式
C12H7BrS2
mdl
——
分子量
295.224
InChiKey
CIVIFDDMHOKBGH-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):
    4.8
  • 重原子数:
    15
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    50.6
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1-bromo-thianthrene正丁基锂乙醚双氧水溶剂黄146 作用下, 生成 5,5,10,10-tetraoxo-5λ6,10λ6-thianthrene-1-carboxylic acid
    参考文献:
    名称:
    Metalation of Thianthrene-5-dioxide by n-Butyllithium and by Phenyllithium and Cleavage of Thianthrene-5,5,10-trioxide by n-Butyllithium
    摘要:
    DOI:
    10.1021/ja01558a055
  • 作为产物:
    描述:
    噻蒽叔丁基锂 作用下, 以 四氢呋喃正戊烷 为溶剂, 以59%的产率得到1-bromo-thianthrene
    参考文献:
    名称:
    Synthesis of 1- and 2-substituted thianthrenes
    摘要:
    噻蒽 C-1 的锂化反应可以合成各种 1-取代的噻蒽,例如噻蒽-1-基硼酸和 1-三丁基锡噻蒽,它们与芳基卤化物发生钯催化偶联反应。通过锂-卤素交换,2-溴噻蒽进入 2-取代噻蒽,然后 2-硫代噻蒽与亲电物反应,包括形成 2-硼酸和 2-三丁基锡噻蒽,并与芳基卤化物偶联。
    DOI:
    10.1039/p19960002391
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文献信息

  • 有机化合物、电子器件及电子装置
    申请人:陕西莱特光电材料股份有限公司
    公开号:CN111004207A
    公开(公告)日:2020-04-14
    本申请涉及一种有机化合物、以及包含该有机化合物的电子器件和包含该电子器件的电子装置。本申请的有机化合物,主体是包含芴或硅芴的稠合杂芳环基,在立体空间中展现为大平面结构,通过在芴或硅芴基的9号位引入富电子的芳胺或杂芳胺取代基,使得化合物的空穴传输性能表现优异。
  • COMPOUND FOR ORGANIC ELECTRIC ELEMENT, ORGANIC ELECTRIC ELEMENT USING SAME, AND ELECTRONIC DEVICE COMPRISING SAME ORGANIC ELECTRONIC ELEMENT
    申请人:DUK SAN NEOLUX CO., LTD.
    公开号:US20190135730A1
    公开(公告)日:2019-05-09
    Provided are an organic electric element and an electronic device comprising the same. According to the present invention, the organic electric element uses a mixture of compounds as a phosphorescent host material which can achieve a high light-emitting efficiency and a low driving voltage and can greatly improve a lifespan in an organic electric element.
    提供了一种有机电子元件及包括该元件的电子设备。根据本发明,该有机电子元件使用化合物混合物作为磷光主体材料,能够实现高发光效率和低驱动电压,并能大大提高有机电子元件的寿命。
  • [EN] AMINOPYRONES AND THEIR USE AS ATM INHIBITORS<br/>[FR] AMINOPYRONES ET LEUR UTILISATION EN TANT QU'INHIBITEURS D'ATM
    申请人:KUDOS PHARM LTD
    公开号:WO2005016919A1
    公开(公告)日:2005-02-24
    Compounds of formula (I) wherein R1 and R2 together form, along with the nitrogen atom to which they are attached, an optionally substituted heterocyclic ring, X is S, NR’’ or CH2, R and R’ are hydrogen or specified substituents, and R’’ is a specified substituent, are useful as inhibitors of the kinase ATM (ataxia-telangiectasia mutated), particularly in the treatment of cancer and retroviral mediated diseases.
    具有式(I)的化合物,其中R1和R2与它们连接的氮原子一起形成一个可选择取代的杂环环,X为S、NR’’或CH2,R和R’为氢或指定的取代基,R’’为一个指定的取代基,可用作激酶ATM(共济失调-毛细血管扩张性疾病突变)的抑制剂,特别是在癌症和逆转录病原体介导的疾病的治疗中。
  • Organometallic Monomers and high Refractive index Polymers derived therefrom
    申请人:Paulasaari Jyri
    公开号:US20140288260A1
    公开(公告)日:2014-09-25
    Synthesis of thianthrene moiety containing silane and germane monomers and their polymerization is presented. The polymers show high refractive index, high transparency and excellent thermal stability. They are useful as dielectric films for semiconductor industry and for optical applications, including high-RI materials in CMOS image sensors.
    本文介绍了含有噻吩基团的硅烷和锗烷单体的合成及其聚合。这些聚合物具有高折射率、高透明度和优异的热稳定性。它们可用作半导体工业的介电膜以及用于光学应用,包括CMOS图像传感器中的高折射率材料。
  • HETEROCYCLIC COMPOUNDS AND THEIR USE IN ELECTRO-OPTICAL OR OPTO-ELECTRONIC DEVICES
    申请人:Power OLEDs Limited
    公开号:US20160035983A1
    公开(公告)日:2016-02-04
    Compounds exhibiting high hole mobility and/or high glass transition temperatures are provided which are of the formula [Ar 1 ] m [Ar 2 ] n wherein: m is an integer from 1-3 and n is an integer and may be 1 or 2; Ar 1 represents a thianthrene residue having a linkage to Ar 2 at one or two positions selected from ring positions 1-4 and 5-8 and optionally mono-, bi- or poly-substituted with C 1 -C 4 -alkyl-, C 1 -C 4 -alkoxy-, fluoro, phenyl or biphenyl which in the case of phenyl or biphenyl may be further substituted with C 1 -C 4 -alkyl-, C 1 -C 4 -alkoxy- or fluoro; Ar 2 represents a residue derived from an arylamine in which the aryl rings are phenyl, naphthyl or anthracenyl optionally substituted with C 1 -C 4 -alkyl-, C 1 -C 4 -alkoxy- or fluoro, a polycyclic fused or chain aromatic ring system optionally containing nitrogen or sulphur and in a chain aromatic ring system optionally containing one or more chain oxygen or sulphur atoms, a triarylphosphine oxide or an arylsilane the rings of any of which are optionally substituted with C 1 -C 4 -alkyl-, C 1 -C 4 -alkoxy- or fluoro. Certain of the compounds may be used in electron transport layers and may be doped with p-type dopants. They may be incorporated into OLEDs, organic photovoltaic devices, imaging members and thin film transistors. In further embodiments there are provided OLEDs or other devices e.g. electrostatic latent image forming members in which improved efficiency is obtained by using as electron transport layers, electron injectors, hosts and emitters (dopants) ambipolar or electron-transmitting compounds in which thianthrene is bonded to aryl e.g. 1-anthracenyl-9-yl-thianthrene, 1-biphenyl-4-yl-thianthrene and 9,10-Bis(1-thianthrenyl) anthracene.
    提供了具有高空穴迁移率和/或高玻璃化转变温度的化合物,其化学式为[Ar1]m[Ar2]n,其中:m为1-3的整数,n为整数,可以为1或2;Ar1代表具有与Ar2连接的噻吩残基,所述连接选择自环位置1-4和5-8的一个或两个位置,并可选择单取代、双取代或多取代于C1-C4烷基、C1-C4烷氧基、氟、苯基或联苯基,其中在苯基或联苯基的情况下,可以进一步取代于C1-C4烷基、C1-C4烷氧基或氟;Ar2代表从芳基胺衍生的残基,其中芳环为苯基、萘基或蒽基,可选择单取代、双取代或多取代于C1-C4烷基、C1-C4烷氧基或氟,多环融合或链芳基环系统可选择包含氮或硫,在链芳基环系统中可选择包含一个或多个链氧或硫原子,三芳基氧化磷或芳基硅烷,其任何环都可选择单取代、双取代或多取代于C1-C4烷基、C1-C4烷氧基或氟。其中某些化合物可用于电子传输层,并可掺杂p型掺杂剂。它们可被纳入OLED、有机光伏器件、成像元件和薄膜晶体管。在进一步的实施例中,提供了使用作为电子传输层、电子注入剂、宿主和发射体(掺杂剂)的双极或电子传输化合物,其中噻吩与芳基(例如1-蒽基-9-基噻吩、1-联苯基-4-基噻吩和9,10-双(1-噻吩基)蒽)结合,从而获得改进的效率的OLED或其他器件,例如静电潜影成像成员。
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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