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1-N,1-N,4-N-triphenyl-4-N-[4-[4-[4-(4-phenyl-N-[4-(N-phenylanilino)phenyl]anilino)phenyl]phenyl]phenyl]benzene-1,4-diamine | 1032984-83-0

中文名称
——
中文别名
——
英文名称
1-N,1-N,4-N-triphenyl-4-N-[4-[4-[4-(4-phenyl-N-[4-(N-phenylanilino)phenyl]anilino)phenyl]phenyl]phenyl]benzene-1,4-diamine
英文别名
——
1-N,1-N,4-N-triphenyl-4-N-[4-[4-[4-(4-phenyl-N-[4-(N-phenylanilino)phenyl]anilino)phenyl]phenyl]phenyl]benzene-1,4-diamine化学式
CAS
1032984-83-0
化学式
C72H54N4
mdl
——
分子量
975.248
InChiKey
OACZPWVYKGIRFV-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):
    19.8
  • 重原子数:
    76
  • 可旋转键数:
    15
  • 环数:
    12.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    13
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENCE DEVICE USING THE SAME
    申请人:YABUNOUCHI Nobuhiro
    公开号:US20080145707A1
    公开(公告)日:2008-06-19
    The present invention provides a novel aromatic amine derivative enabling to obtain an organic electroluminescence device which is driven under a low voltage, exhibits small increase in the driving voltage after continuous driving for a long time and has a long life. The amine derivative is represented by the following general formula (1). In the formula, R 1 to R 7 each represent, for example, hydrogen atom or a substituted or unsubstituted aryl group having 5 to 50 nuclear carbon atoms; a represents an integer of 1 or greater; b, c, g and h each represent an integer of 1 to 5, and d, e and f each represent an integer of 1 to 4; and Ar 1 and Ar 2 represent a group represented by following general formulae (2) and (3), respectively, and the groups represented by Ar 1 and Ar 2 are not same with each other. R 8 to R 11 each represent, for example, hydrogen atom; and i and m each represent an integer of 1 to 5, j and k each represent an integer of 1 to 4, n and p each represent an integer of 0 or greater, and n≠p.
    本发明提供了一种新的芳香胺衍生物,使得可以获得一种在低电压下驱动的有机电致发光器件,其在连续驱动长时间后驱动电压的增加很小,并且具有长寿命。该胺衍生物由以下通式(1)表示。在该式中,R1至R7分别表示氢原子或具有5到50个核碳原子的取代或未取代芳基基团;a表示大于或等于1的整数;b、c、g和h分别表示1到5的整数,d、e和f分别表示1到4的整数;Ar1和Ar2分别表示由以下通式(2)和(3)表示的基团,且由Ar1和Ar2表示的基团不相同。R8至R11分别表示氢原子;i和m分别表示1到5的整数,j和k分别表示1到4的整数,n和p分别表示大于或等于0的整数,且n≠p。
  • Aza-Residue Modulation of Cyclic <scp>d</scp>,<scp>l</scp>-α-Peptide Nanotube Assembly with Enhanced Anti-Amyloidogenic Activity
    作者:Maram Habashi、Pradeep S. Chauhan、Suresh Vutla、Sudipta Senapati、Mykhailo Diachkov、Ali EL-Husseini、Brigitte Guérin、William D. Lubell、Shai Rahimipour
    DOI:10.1021/acs.jmedchem.2c02049
    日期:2023.2.23
    Transient soluble oligomers of amyloid-β (Aβ) are considered among the most toxic species in Alzheimer’s disease (AD). Solubleoligomers accumulate early prior to insoluble plaque formation and cognitive impairment. The cyclic d,l-α-peptide CP-2 (1) self-assembles into nanotubes and demonstrates promising anti-amyloidogenic activity likely by a mechanism involving engagement of soluble oligomers. Systematic
    淀粉样蛋白-β (Aβ) 的瞬时可溶性低聚物被认为是阿尔茨海默病 (AD) 中毒性最强的物种之一。可溶性 Aβ 寡聚体在不溶性斑块形成和认知障碍之前早期积累。环状d , l -α-肽 CP-2 ( 1 ) 自组装成纳米管并显示出有前途的抗淀粉样蛋白生成活性,这可能是通过涉及可溶性低聚物参与的机制实现的。肽1中残基的系统置换与氮杂氨基酸对应物进行了探索氢键对减轻 Aβ 聚集和毒性的倾向的影响。某些氮杂肽表现出提高的参与、改变二级结构和抑制 Aβ 聚集的能力。此外,某些氮杂肽可分解预先形成的 Aβ 原纤维并保护细胞免受 Aβ 介导的毒性。用氮杂正亮酸和氮杂高丝氨酸分别取代肽1中的l -正亮酸3和d -丝氨酸6残基,提供无毒的 [azaNle 3 ]- 1 ( 4 ) 和 [azaHse 6 ]- 1 ( 7), 通过降低 Aβ 寡聚体平显着减轻转基因秀丽隐杆线虫AD 模型的症状。
  • ORGANIC ELECTROLUMINESCENCE DEVICE
    申请人:Jinde Yukitoshi
    公开号:US20100301312A1
    公开(公告)日:2010-12-02
    An organic electroluminescence device including: an anode ( 10 ), a cathode ( 70 ), an emitting layer ( 40 ) including an organic compound, which is between the anode ( 10 ) and the cathode ( 70 ), two or more layers arranged in a hole injection and transport region which is between the anode ( 10 ) and the emitting layer ( 40 ), and one or more layers arranged in an electron injection and transport region which is between the emitting layer ( 40 ) and the cathode ( 70 ), wherein a layer in the hole injection and transport region, which is in contact with the emitting layer ( 40 ), includes an aromatic amine derivative having a carbazole skeleton, one of the layers other than the layer in contact with the emitting layer ( 40 ) in the hole injection and transport region includes one or more materials selected from the group consisting of thiophene derivatives, tricyclic or more cyclic fused aromatic derivatives, amine derivatives excluding the compound represented by the following formula (A), conductive polymers, CF x , CuPc, transition metal oxides, fullerenes and acceptor materials, and a layer in the electron injection and transport region includes a benzimidazole derivative.
  • US9174938B2
    申请人:——
    公开号:US9174938B2
    公开(公告)日:2015-11-03
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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