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

RJC 03105 | 144603-11-2

中文名称
——
中文别名
——
英文名称
RJC 03105
英文别名
7,8-dichloro-4-hydroxy-3-phenyl-1H-quinolin-2-one
RJC 03105化学式
CAS
144603-11-2
化学式
C15H9Cl2NO2
mdl
——
分子量
306.148
InChiKey
FBCPIPFPVLTJCV-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:
    520.0±50.0 °C(Predicted)
  • 密度:
    1.507±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.6
  • 重原子数:
    20
  • 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:
    49.3
  • 氢给体数:
    2
  • 氢受体数:
    2

SDS

SDS:f6e49b679a19fcb6926acdc0cff1406c
查看

反应信息

  • 作为反应物:
    描述:
    RJC 03105磺酰氯 作用下, 以 1,4-二氧六环 为溶剂, 反应 0.17h, 以79%的产率得到3,7,8-trichloro-3-phenyl-1H-quinoline-2,4-dione
    参考文献:
    名称:
    Halogenation reactions in position 3 of quinoline-2,4-dione systems by electrophilic substitution and halogen exchange
    摘要:
    3-Substituted 4-hydroxy-2(1 H)-quinolones 3, 5, 7 are halogenated with bromine or sulfuryl chloride to yield the quinolinediones 9 or 10. Reaction of 3, 5, 7 with chloroform gives the dichloromethyl quinolinediones 11. Halogen exchange leads from the chloro quinolinediones 10 to fluoro quinolinedones 12 and to azido quinolinediones 13. Similarly the dichloro quinolinedione 10 an reacts to the difluoro quinolinedione 14, which is reduced to the 3-fluoro-4-hydroxyquinolone 16 and reacts again with sulfuryl chloride to give the mixed 3-chloro-3-fluoroquinolinedione 15.
    DOI:
    10.1007/bf00816857
  • 作为产物:
    描述:
    2,3-二氯苯胺苯基丙二酸二乙酯 反应 4.0h, 以90%的产率得到RJC 03105
    参考文献:
    名称:
    Halogenation reactions in position 3 of quinoline-2,4-dione systems by electrophilic substitution and halogen exchange
    摘要:
    3-Substituted 4-hydroxy-2(1 H)-quinolones 3, 5, 7 are halogenated with bromine or sulfuryl chloride to yield the quinolinediones 9 or 10. Reaction of 3, 5, 7 with chloroform gives the dichloromethyl quinolinediones 11. Halogen exchange leads from the chloro quinolinediones 10 to fluoro quinolinedones 12 and to azido quinolinediones 13. Similarly the dichloro quinolinedione 10 an reacts to the difluoro quinolinedione 14, which is reduced to the 3-fluoro-4-hydroxyquinolone 16 and reacts again with sulfuryl chloride to give the mixed 3-chloro-3-fluoroquinolinedione 15.
    DOI:
    10.1007/bf00816857
点击查看最新优质反应信息

文献信息

  • Agents And Methods For Treating Ischemic And Other Diseases
    申请人:Sun Xiujun
    公开号:US20140221423A1
    公开(公告)日:2014-08-07
    This invention relates to compounds that modulate TRPM7 protein activity and use of the same for treatment or prophylaxis of ischemia, cancer, pain or glaucoma.
    本发明涉及调节TRPM7蛋白活性的化合物及其在缺血、癌症、疼痛或青光眼的治疗或预防中的应用。
  • US9334256B2
    申请人:——
    公开号:US9334256B2
    公开(公告)日:2016-05-10
  • US9566284B2
    申请人:——
    公开号:US9566284B2
    公开(公告)日:2017-02-14
  • Halogenation reactions in position 3 of quinoline-2,4-dione systems by electrophilic substitution and halogen exchange
    作者:Wolfgang Stadlbauer、Rita Laschober、Herbert Lutschouig、Gerda Schindler、Thomas Kappe
    DOI:10.1007/bf00816857
    日期:——
    3-Substituted 4-hydroxy-2(1 H)-quinolones 3, 5, 7 are halogenated with bromine or sulfuryl chloride to yield the quinolinediones 9 or 10. Reaction of 3, 5, 7 with chloroform gives the dichloromethyl quinolinediones 11. Halogen exchange leads from the chloro quinolinediones 10 to fluoro quinolinedones 12 and to azido quinolinediones 13. Similarly the dichloro quinolinedione 10 an reacts to the difluoro quinolinedione 14, which is reduced to the 3-fluoro-4-hydroxyquinolone 16 and reacts again with sulfuryl chloride to give the mixed 3-chloro-3-fluoroquinolinedione 15.
查看更多