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8-氯-6-羟基喹啉 | 18119-24-9

中文名称
8-氯-6-羟基喹啉
中文别名
6-羟基-8-氯喹啉;6-氯-8-羟基喹啉
英文名称
8-chloro-6-hydroxyquinoline
英文别名
8-Chlor-6-hydroxychinolin;8-chloro-quinolin-6-ol;8-Chlor-chinolin-6-ol;8-Chloroquinolin-6-OL
8-氯-6-羟基喹啉化学式
CAS
18119-24-9
化学式
C9H6ClNO
mdl
MFCD09951943
分子量
179.606
InChiKey
NSFZSTFINAEFAB-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

  • 熔点:
    237-238 °C (decomp)(Solv: ethanol (64-17-5))
  • 沸点:
    343.5±22.0 °C(Predicted)
  • 密度:
    1.412±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    33.1
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933499090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319
  • 储存条件:
    室温

SDS

SDS:efc849bc90cca543c869f71a8ea76188
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Piperazine-piperidine antagonists and agonists of the 5-HT1A receptor
    申请人:Asselin Magda
    公开号:US20070027160A1
    公开(公告)日:2007-02-01
    The present invention relates to novel piperazine-piperidine compounds. The compounds are useful as 5-HT 1A binding agents, particularly as 5-HT 1A receptor antagonists and agonists. These compounds are useful in treating central nervous system disorders, such as cognition disorders, anxiety disorders, depression and sexual dysfunction.
    本发明涉及新型哌嗪-哌啶化合物。这些化合物可用作5-HT1A结合剂,特别是作为5-HT1A受体拮抗剂和激动剂。这些化合物在治疗中枢神经系统疾病方面很有用,如认知障碍、焦虑症、抑郁症和性功能障碍。
  • BENZOFURANYL- AND BENZOTHIENYL- PIPERAZINYL QUINOLINES AND METHODS OF THEIR USE
    申请人:Venkatesan Aranapakam Mudumbai
    公开号:US20090054454A1
    公开(公告)日:2009-02-26
    Benzofuranyl- and benzothienyl-piperzinyl quinoline derivatives and compositions containing such compounds are disclosed. Methods of using benzofuranyl- and benzothienyl-piperzinyl quinoline derivatives and compositions containing such composition in the treatment and/or prevention of serotonin-related disorders, such as depression and anxiety, are also disclosed. In addition, processes for the preparation of benzofuranyl- and benzothienyl-piperzinyl quinoline derivatives are disclosed.
    本专利揭示了苯并呋喃基和苯并噻吩基哌嗪喹啉衍生物以及含有这些化合物的组合物。还揭示了使用苯并呋喃基和苯并噻吩基哌嗪喹啉衍生物以及含有这种组合物在治疗和/或预防与5-羟色胺相关的疾病,如抑郁症和焦虑症的方法。此外,还揭示了制备苯并呋喃基和苯并噻吩基哌嗪喹啉衍生物的方法。
  • 6-Methoxy-8-[4-(1-(5-fluoro)-quinolin-8-yl-piperidin-4-yl)-piperazin-1-yl]-quinoline hydrochloric acid salts
    申请人:Schmid Jean
    公开号:US20070299083A1
    公开(公告)日:2007-12-27
    The present invention relates to hydrochloric acid salt and crystalline forms of the 5-HT 1A binding agent 6-methoxy-8-[4-(1-(5-fluoro)-quinolin-8-yl-piperidin-4-yl)-piperazin-1-yl]-quinoline, as well as pharmaceutical compositions thereof, and methods of use thereof.
    本发明涉及盐酸盐和结晶形式的5-HT1A结合剂6-甲氧基-8-[4-(1-(5-氟基)-喹诺啉-8-基-哌啶-4-基)-哌嗪-1-基]-喹啉,以及其药物组合物和使用方法。
  • Benzofuranyl-and benzothienyl-piperazinyl quinolines and methods of their use
    申请人:Venkatesan Mudumbai Aranapakam
    公开号:US20050059673A1
    公开(公告)日:2005-03-17
    Benzofuranyl- and benzothienyl-piperzinyl quinoline derivatives and compositions containing such compounds are disclosed. Methods of using benzofuranyl- and benzothienyl-piperzinyl quinoline derivatives and compositions containing such composition in the treatment and/or prevention of serotonin-related disorders, such as depression and anxiety, are also disclosed. In addition, processes for the preparation of benzofuranyl- and benzothienyl-piperzinyl quinoline derivatives are disclosed.
    本发明涉及苯并呋喃基-和苯并噻吩基-哌嗪基喹啉衍生物及含有该类化合物的组合物。本发明还涉及使用苯并呋喃基-和苯并噻吩基-哌嗪基喹啉衍生物及含有该类组合物治疗和/或预防与血清素相关的疾病,例如抑郁和焦虑。此外,还公开了制备苯并呋喃基-和苯并噻吩基-哌嗪基喹啉衍生物的方法。
  • Crystalline forms of 6-methoxy-8-[4-(1-(5-fluoro)-quinolin-8-yl-piperidin-4-yl)-piperazin-1-yl]-quinoline
    申请人:Bicksler James J.
    公开号:US20080119481A1
    公开(公告)日:2008-05-22
    The present invention relates to crystalline forms of the 5-HT 1A binding agent 6-methoxy-8-[4-(1-(5-fluoro)-quinolin-8-yl-piperidin-4-yl)-piperazin-1-yl]-quinoline, as well as pharmaceutical compositions thereof, and methods of use thereof.
    本发明涉及5-HT1A结合剂6-甲氧基-8-[4-(1-(5-氟)-喹啉-8-基哌啶-4-基)-哌嗪-1-基]-喹啉的晶体形式,以及其制备的制药组合物和使用方法。
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