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(S)-3-phenoxypyrrolidine | 931581-76-9

中文名称
——
中文别名
——
英文名称
(S)-3-phenoxypyrrolidine
英文别名
(3S)-3-phenoxypyrrolidine
(S)-3-phenoxypyrrolidine化学式
CAS
931581-76-9
化学式
C10H13NO
mdl
MFCD08688473
分子量
163.219
InChiKey
SKHPQIQATRHESG-JTQLQIEISA-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:
    259.2±33.0 °C(Predicted)
  • 密度:
    1.058±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    21.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933990090

反应信息

  • 作为反应物:
    描述:
    (S)-3-phenoxypyrrolidine 、 5-(2,4,5-trifluoro-3-hydroxyphenyl)-1,2,4-oxadiazole-3-carboxylic acid 在 N,N-二异丙基乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以6 %的产率得到(S)-(3-phenoxypyrrolidin-1-yl)(5-(2,4,5-trifluoro-3-hydroxyphenyl)-1,2,4-oxadiazol-3-yl)methanone
    参考文献:
    名称:
    WO2023/222850
    摘要:
    公开号:
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文献信息

  • PHENYL-(AZA)CYCLOALKYL CARBOXYLIC ACID GPR120 MODULATORS
    申请人:BRISTOL-MYERS SQUIBB COMPANY
    公开号:US20170327457A1
    公开(公告)日:2017-11-16
    The present invention provides compounds of Formula (I): or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein all of the variables are as defined herein. These compounds are GPR120 G protein-coupled receptor modulators which may be used as medicaments.
  • 1,2,4-Triazolo [4,3-A] Pyridine Derivatives And Their Use For The Treatment Of Prevention Of Neurological And Psychiatric Disorders
    申请人:JANSSEN PHARMACEUTICALS, INC.
    公开号:US20170333426A1
    公开(公告)日:2017-11-23
    The present invention relates to methods of treating various central nervous system disorders using novel triazolo[4,3-a]pyridine derivatives of Formula (I) wherein all radicals are as defined in the claims. The compounds according to the invention are positive allosteric modulators of the metabotropic glutamate receptor subtype 2 (“mGluR2”), which are useful for the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction and diseases in which the mGluR2 subtype of metabotropic receptors is involved. The invention is also directed to pharmaceutical compositions comprising such compounds, to processes to prepare such compounds and compositions, and to the use of such compounds for the prevention or treatment of neurological and psychiatric disorders and diseases in which mGluR2 is involved.
  • US8415350B2
    申请人:——
    公开号:US8415350B2
    公开(公告)日:2013-04-09
  • US9737533B2
    申请人:——
    公开号:US9737533B2
    公开(公告)日:2017-08-22
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