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1-ethyl-3-(trifluoromethyl)-4,5-dihydro-1H-pyrazol-5-one | 866472-53-9

中文名称
——
中文别名
——
英文名称
1-ethyl-3-(trifluoromethyl)-4,5-dihydro-1H-pyrazol-5-one
英文别名
2-ethyl-5-(trifluoromethyl)-4H-pyrazol-3-one
1-ethyl-3-(trifluoromethyl)-4,5-dihydro-1H-pyrazol-5-one化学式
CAS
866472-53-9
化学式
C6H7F3N2O
mdl
MFCD12026378
分子量
180.13
InChiKey
NESMTDYSHSBSJX-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:
    128.3±50.0 °C(Predicted)
  • 密度:
    1.42±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.666
  • 拓扑面积:
    32.7
  • 氢给体数:
    0
  • 氢受体数:
    5

文献信息

  • BENZOXAZINE DERIVATIVES AS CRAC MODULATORS
    申请人:Hoffmann-La Roche Inc.
    公开号:US20130090333A1
    公开(公告)日:2013-04-11
    Compounds of the formula (I): or pharmaceutically acceptable salts thereof, wherein R 1 and R 2 are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of diseases associated with calcium release-activated calcium channels (CRAC).
    公式(I)的化合物: 或其药用可接受的盐,其中R1和R2如本文所述定义。还公开了制造这些化合物的方法以及使用这些化合物治疗与释放激活通道(CRAC)相关疾病的用途。
  • AZABENZOXAZINE DERIVATIVES AS CRAC MODULATORS
    申请人:Hoffmann-La Roche Inc
    公开号:US20130090334A1
    公开(公告)日:2013-04-11
    Compounds of the formula (I): or pharmaceutically acceptable salts thereof, wherein R 1 and R 2 are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of diseases associated with calcium release-activated calcium channels (CRAC).
    公式(I)的化合物: 或其药用可接受的盐,其中R1和R2如本文所述定义。还公开了制造这些化合物的方法以及使用这些化合物治疗与释放激活通道(CRAC)相关疾病的用途。
  • 7-AZAINDOLE INHIBITORS OF CRAC
    申请人:Hoffmann-La Roche Inc.
    公开号:US20130158049A1
    公开(公告)日:2013-06-20
    Disclosed are compounds of Formula (I): useful for treatment of autoimmune and inflammatory diseases associated with IL-2 inhibition via modulation of calcium release-activated calcium (CRAC) channels. Also disclosed are methods of making and using the compounds for treatment of diseases associated with CRAC channels.
    公开了公式(I)的化合物: 用于治疗与IL-2抑制有关的自身免疫和炎症性疾病,通过调节释放激活(CRAC)通道。还公开了制造和使用这些化合物用于治疗与CRAC通道相关的疾病的方法。
  • INDOLE DERIVATIVES AS CRAC MODULATORS
    申请人:Alam Muzaffar
    公开号:US20110071150A1
    公开(公告)日:2011-03-24
    Compounds of the formula I: or pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , R 3 and R 4 are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of diseases associated with calcium release-activated calcium channels (CRAC).
    公式I的化合物: 或其药用可接受的盐, 其中R1、R2、R3和R4按本文定义。还公开了制造这些化合物的方法以及使用这些化合物治疗与释放激活通道(CRAC)相关疾病的用途。
  • DIAZAINDOLE INHIBITORS OF CRAC
    申请人:Hoffmann-La Roche Inc.
    公开号:US20130158040A1
    公开(公告)日:2013-06-20
    Disclosed are compounds of Formula (I): useful for treatment of autoimmune and inflammatory diseases associated with IL-2 inhibition via modulation of calcium release-activated calcium (CRAC) channels. Also disclosed are methods of making and using the compounds for treatment of diseases associated with CRAC channels.
    公开了公式(I)的化合物: 用于治疗与IL-2抑制有关的自身免疫和炎症性疾病,通过调节释放激活(CRAC)通道。还公开了制造和使用这些化合物用于治疗与CRAC通道相关的疾病的方法。
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