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2,2,2-trifluoro-N-[1-(1H-imidazol-5-yl)-3-oxopentan-2-yl]acetamide | 258260-91-2

中文名称
——
中文别名
——
英文名称
2,2,2-trifluoro-N-[1-(1H-imidazol-5-yl)-3-oxopentan-2-yl]acetamide
英文别名
——
2,2,2-trifluoro-N-[1-(1H-imidazol-5-yl)-3-oxopentan-2-yl]acetamide化学式
CAS
258260-91-2
化学式
C10H12F3N3O2
mdl
——
分子量
263.219
InChiKey
JVNCXLIHHSQTSG-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):
    1
  • 重原子数:
    18
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    74.8
  • 氢给体数:
    2
  • 氢受体数:
    6

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

反应信息

  • 作为反应物:
    描述:
    2,2,2-trifluoro-N-[1-(1H-imidazol-5-yl)-3-oxopentan-2-yl]acetamide劳森试剂 作用下, 以 甲苯 为溶剂, 生成 5-ethyl-4-(1H-imidazol-5-ylmethyl)-2-(trifluoromethyl)-1,3-thiazole
    参考文献:
    名称:
    α2 Adrenoceptor Agonists as Potential Analgesic Agents. 1. (Imidazolylmethyl)oxazoles and -thiazoles
    摘要:
    A series of (imidazolylmethyl)oxazoles and -thiazoles were prepared and evaluated as alpha(2) adrenoceptor agonists. These compounds were also tested in in vivo paradigms that are predictive of analgesic activity. Variations in both the imidazole and thiazole portions of the molecule were investigated. Some of the more potent compounds such as 22, 26, 45, and 53 displayed at receptor binding in the 10-20 nM range and also had significant, antinociceptive activity in the mouse abdominal irritant test (MAIT).
    DOI:
    10.1021/jm990005a
  • 作为产物:
    参考文献:
    名称:
    α2 Adrenoceptor Agonists as Potential Analgesic Agents. 1. (Imidazolylmethyl)oxazoles and -thiazoles
    摘要:
    A series of (imidazolylmethyl)oxazoles and -thiazoles were prepared and evaluated as alpha(2) adrenoceptor agonists. These compounds were also tested in in vivo paradigms that are predictive of analgesic activity. Variations in both the imidazole and thiazole portions of the molecule were investigated. Some of the more potent compounds such as 22, 26, 45, and 53 displayed at receptor binding in the 10-20 nM range and also had significant, antinociceptive activity in the mouse abdominal irritant test (MAIT).
    DOI:
    10.1021/jm990005a
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