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8-(2,4-dichlorophenyl)-2,7-dimethyl-1H-quinolin-4-one | 620179-01-3

中文名称
——
中文别名
——
英文名称
8-(2,4-dichlorophenyl)-2,7-dimethyl-1H-quinolin-4-one
英文别名
——
8-(2,4-dichlorophenyl)-2,7-dimethyl-1H-quinolin-4-one化学式
CAS
620179-01-3
化学式
C17H13Cl2NO
mdl
——
分子量
318.202
InChiKey
HIBLTPHYZVPCJR-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

  • 沸点:
    437.6±40.0 °C(Predicted)
  • 密度:
    1.342±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.53
  • 重原子数:
    21.0
  • 可旋转键数:
    1.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    33.12
  • 氢给体数:
    1.0
  • 氢受体数:
    2.0

上下游信息

  • 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:
    参考文献:
    名称:
    Synthesis and SAR of 8-Arylquinolines as potent corticotropin-Releasing factor1 (CRF1) receptor antagonists
    摘要:
    A series of 4-substituted 8-aryl-2-methylquinolines 4 was designed and synthesized as highly potent antagonists for the human CRF1 receptor. This series of compounds displayed parallel SAR to other bicyclic systems such as pyrazolo[l,5-a]pyrimidines, with several compounds possessing low nanomolar binding affinity. In addition to the high potency, the basicity of this 4-aminoquinoline core may offer CRF1 antagonists with lower lipophilicity. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(03)00684-x
  • 作为产物:
    参考文献:
    名称:
    Synthesis and SAR of 8-Arylquinolines as potent corticotropin-Releasing factor1 (CRF1) receptor antagonists
    摘要:
    A series of 4-substituted 8-aryl-2-methylquinolines 4 was designed and synthesized as highly potent antagonists for the human CRF1 receptor. This series of compounds displayed parallel SAR to other bicyclic systems such as pyrazolo[l,5-a]pyrimidines, with several compounds possessing low nanomolar binding affinity. In addition to the high potency, the basicity of this 4-aminoquinoline core may offer CRF1 antagonists with lower lipophilicity. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(03)00684-x
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