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2--perimidin | 24216-46-4

中文名称
——
中文别名
——
英文名称
2--perimidin
英文别名
2-pyridin-4-yl-1H-perimidine;2-(4-pyridinyl)-1H-perimidine;2-pyridin-4-yl-1H-perimidine
2-<Pyridyl-(4)>-perimidin化学式
CAS
24216-46-4
化学式
C16H11N3
mdl
——
分子量
245.283
InChiKey
IHRUYMZEEDZGCC-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):
    2.6
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • AZAPYRENES FOR ELECTRONIC APPLICATIONS
    申请人:BASF SE
    公开号:EP2313472B1
    公开(公告)日:2012-08-15
  • Novel pharmaceutical and diagnostic compositions for use in the treatment and diagnosis of neurodegenerative diseases or amyloid diseases
    申请人:Wanker Erich
    公开号:US20090117040A1
    公开(公告)日:2009-05-07
    The present invention relates to pharmaceutical and diagnostic compositions as well as to the use of the active substances contained therein for preparing a pharmaceutical or a diagnostic composition for the treatment or diagnosis of neurodegenerative disorders or amyloid diseases.
  • US8193528B2
    申请人:——
    公开号:US8193528B2
    公开(公告)日:2012-06-05
  • [EN] AZAPYRENES FOR ELECTRONIC APPLICATIONS<br/>[FR] AZAPYRÈNES POUR DES APPLICATIONS ÉLECTRONIQUES
    申请人:BASF SE
    公开号:WO2010006890A1
    公开(公告)日:2010-01-21
    The present invention relates to electronic devices, especially electroluminescent devices, comprising azapyrenes of formula (I), or formula (III), wherein Y1, Y2, Y3, Y4, X1, X2 and X3 are independently each other N, or CR4, with the proviso that at least one of the groups X1, X2 and X3 is a group CR4, R1 is hydrogen, F, -SiR100R101R102, or an organic substituent, R4 is hydrogen, F, -SiR100R101R102, or an organic substituent, or any of the substituents R1, R1' and R4, which are adjacent to each other, together form an aromatic, or heteroaromatic ring, or ring system, which can optionally be substituted, m is an integer of 1 to 6, and R100, R101 and R102 are independently of each other a C1-C8alkyl group, a C6-C24aryl group, or a C7-C12aralkylgroup, which may optionally be substituted, and Q is a linking group; with the proviso that in the compound of formula (III) at least one of the substituents R1, or R4 is a group Q; especially as host for phosphorescent emitters, electron transporting materials, or emitter materials. The hosts may function with phosphorescent materials to provide improved efficiency, stability, manufacturability, or spectral characteristics of electroluminescent devices.
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