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7-chloro-2-(3-fluorophenyl)-1H-quinolin-4-one | 958752-63-1

中文名称
——
中文别名
——
英文名称
7-chloro-2-(3-fluorophenyl)-1H-quinolin-4-one
英文别名
——
7-chloro-2-(3-fluorophenyl)-1H-quinolin-4-one化学式
CAS
958752-63-1
化学式
C15H9ClFNO
mdl
——
分子量
273.694
InChiKey
QAJWIFHUECFWDX-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):
    3.9
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    potassium carbonate 作用下, 以 甲醇 为溶剂, 反应 96.0h, 生成 7-chloro-2-(3-fluorophenyl)-1H-quinolin-4-one
    参考文献:
    名称:
    Synthesis of a quinolone library from ynones
    摘要:
    A library of 72 quinolones was synthesized from substituted anthranilic acids, using ynone intermediates. These masked beta-dicarbonyl synthons allowed cyclization under milder conditions than previously reported quinolone syntheses. (C) 2009 Elsevier Ltd. All rights reserved
    DOI:
    10.1016/j.tetlet.2009.09.024
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文献信息

  • COMPOSITIONS AND METHODS FOR MONITORING, DIAGNOSIS, PROGNOSIS, DETECTION, AND TREATMENT OF CANCER
    申请人:Shrivastava Shivani
    公开号:US20220168422A1
    公开(公告)日:2022-06-02
    The present invention relates to the use of compositions for treating or preventing a cancer condition in a subject. The use of composition comprises methods of treating or preventing cancer with agents that inhibit Nanog expression and/or activity. The pharmaceutical composition will further comprise agents that inhibit Nanog expression or activity in a subject.
  • Synthesis of a quinolone library from ynones
    作者:Timothy R. Ward、Brandon J. Turunen、Torsten Haack、Benjamin Neuenswander、William Shadrick、Gunda I. Georg
    DOI:10.1016/j.tetlet.2009.09.024
    日期:2009.11
    A library of 72 quinolones was synthesized from substituted anthranilic acids, using ynone intermediates. These masked beta-dicarbonyl synthons allowed cyclization under milder conditions than previously reported quinolone syntheses. (C) 2009 Elsevier Ltd. All rights reserved
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