摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4'-iodo-m-terphenyl | 64896-41-9

中文名称
——
中文别名
——
英文名称
4'-iodo-m-terphenyl
英文别名
2,4-diphenyl benzene iodide;4'-Iod-m-terphenyl;4'-Jod-m-terphenyl;1-Iodo-2,4-diphenylbenzene
4'-iodo-m-terphenyl化学式
CAS
64896-41-9
化学式
C18H13I
mdl
——
分子量
356.206
InChiKey
FDBCMONOPQQOAG-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:
    38-40 °C
  • 沸点:
    168-170 °C(Press: 0.01 Torr)
  • 密度:
    1.471±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.8
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

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
  • 下游产品
    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:
    4'-iodo-m-terphenyl高碘酸 作用下, 反应 19.0h, 生成 4,4'-Diiodo-m-terphenyl
    参考文献:
    名称:
    Rabilloud,G. et al., Bulletin de la Societe Chimique de France, 1977, p. 281 - 287
    摘要:
    DOI:
  • 作为产物:
    参考文献:
    名称:
    The Halogenation of m-Diphenylbenzene. II. The Monoiodo Derivative1
    摘要:
    DOI:
    10.1021/ja01262a076
点击查看最新优质反应信息

文献信息

  • CONDENSED CYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME
    申请人:Samsung Display Co., Ltd.
    公开号:US20190131540A1
    公开(公告)日:2019-05-02
    Provided are a condensed cyclic compound represented by the following formulas and an organic light-emitting device including the same. The organic lightemitting device includes a first electrode; a second electrode facing the first electrode, and an organic layer between the first electrode and the second electrode, where the organic layer includes an emission layer and at least one of the condensed cyclic compound described above.
    提供了由以下公式表示的简化环状化合物和包括该化合物的有机发光器件。该有机发光器件包括第一电极;面向第一电极的第二电极,以及位于第一电极和第二电极之间的有机层,其中有机层包括发射层和上述简化环状化合物中的至少一个。
  • PHOTOELECTRIC CONVERSION ELEMENT, AND IMAGE SENSOR, SOLAR CELL, SINGLE COLOR DETECTION SENSOR AND FLEXIBLE SENSOR EACH OF WHICH USES SAID PHOTOELECTRIC CONVERSION ELEMENT
    申请人:TORAY INDUSTRIES, INC.
    公开号:US20170141320A1
    公开(公告)日:2017-05-18
    The present invention has the configuration described below for the purpose of providing a photoelectric conversion efficiency element which exhibits high charge mobility, while having high photoelectric conversion efficiency. A photoelectric conversion element which comprises at least one organic layer between a first electrode and a second electrode, and which is characterized in that the organic layer contains a first compound represented by general formula (1) and a second compound that has a maximum value of absorption coefficient of 5×10 4 cm −1 or more at a wavelength of 400-700 nm.
    为了提供一种具有高电荷迁移率和高光电转换效率的光电转换效率元件,本发明具有以下所述的配置。一种光电转换元件,其包括第一电极和第二电极之间至少一个有机层,并且其特征在于有机层包含由通式(1)表示的第一化合物和在波长为400-700 nm处具有吸收系数最大值为5×10^4 cm^-1或更大的第二化合物。
  • ORGANOMETALLIC COMPOUND, ORGANIC LIGHT-EMITTING DEVICE INCLUDING ORGANOMETALLIC COMPOUND AND ELECTRONIC APPARATUS INCLUDING THE ORGANIC LIGHT-EMITTING DEVICE
    申请人:Samsung Electronics Co., Ltd.
    公开号:US20210171548A1
    公开(公告)日:2021-06-10
    Provided are an organometallic compound represented by Formula 1, an organic light-emitting device including the organometallic compound and an electronic apparatus including the organic light-emitting device: Formula 1 may be understood by referring to the descriptions of Formula 1 provided herein.
    提供的是由化学式1表示的有机属化合物,包括该有机属化合物的有机发光器件和包括该有机发光器件的电子设备:化学式1可通过参考此处提供的化学式1的描述来理解。
  • ORGANIC ELECTROLUMINESCENCE DEVICE
    申请人:Sado Takayasu
    公开号:US20080290795A1
    公开(公告)日:2008-11-27
    Provided is an organic electroluminescence device in which a reduction in luminance is suppressed and a lifetime is significantly improved. The object is achieved by an organic electroluminescence device having organic compound layers including an organic emitting layer, which is interposed between at least one pair of electrodes, in which the organic emitting layer is formed of an organic compound material containing an impurity composed of a hydroxyl group-containing compound at a concentration of less than 0.15% by mass, and a method of selecting an organic compound material for the organic electroluminescence device, the method including: determining the content of the impurity; and selecting an organic compound material in which the content is less than 0.15% by mass so that the material is used for forming the organic emitting layer. Provided are a coating film-forming ink, a method of forming a thin film, and a method of producing an organic electroluminescence device.
    提供了一种有机电致发光器件,其中抑制了亮度降低并显著提高了寿命。该目标通过具有有机化合物层的有机电致发光器件实现,其中有机发光层位于至少一对电极之间,有机发光层由含有羟基化合物组成的杂质浓度低于0.15%的有机化合物材料形成,以及选择有机化合物材料用于有机电致发光器件的方法,该方法包括:确定杂质的含量;选择杂质含量低于0.15%的有机化合物材料,以便用于形成有机发光层。还提供了一种涂层膜形成油墨、一种薄膜形成方法和一种有机电致发光器件的生产方法。
  • NAPHTHACENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME
    申请人:Idemitsu Kosan Co., Ltd.
    公开号:EP1990332A1
    公开(公告)日:2008-11-12
    A material for an organic EL device conatining a novel naphthacene derivative; a luminescent material conatining a novel naphthacene derivative; and an organic electroluminescence device including one or more organic layers interposed between a cathode and an anode, and at least one layer of the organic layers containing a naphthacene derivative represented by the following formula (1) or (2).
    一种含有新型生物的有机电致发光器件材料;一种含有新型生物发光材料;以及一种有机电致发光器件,该器件包括一个或多个插在阴极和阳极之间的有机层,其中至少有一层有机层含有下式(1)或(2)代表的生物
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫