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1-(4-methylphenyl)-4,5,6,7-tetrahydroindazole-3-carboxylic acid | 223444-60-8

中文名称
——
中文别名
——
英文名称
1-(4-methylphenyl)-4,5,6,7-tetrahydroindazole-3-carboxylic acid
英文别名
1-(4-methylphenyl)-4,5,6,7-tetrahydro-1H-indazole-3-carboxylic acid
1-(4-methylphenyl)-4,5,6,7-tetrahydroindazole-3-carboxylic acid化学式
CAS
223444-60-8
化学式
C15H16N2O2
mdl
MFCD09048804
分子量
256.304
InChiKey
LWLMKQSNSUNIGG-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):
    3.3
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.333
  • 拓扑面积:
    55.1
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    1-(4-methylphenyl)-4,5,6,7-tetrahydroindazole-3-carboxylic acid氯化亚砜 作用下, 以 为溶剂, 反应 1.0h, 以96%的产率得到1-(4-methylphenyl)-3-chlorocarbonyl-4,5,6,7-tetrahydroindazole
    参考文献:
    名称:
    New cycloalkylpyrazoles as potential cyclooxygenase inhibitors
    摘要:
    In this study some cycloalkyl-3-(N-substituted carbamoyl)-1-phenylpyrazoles have been synthesized in order to screen their capability to inhibit human cyclooxygenase. The synthetic pathway is based on the well known property of nitrilimines to undergo 1,3-dipolar cycloaddition reactions. The structures of all the synthesized compounds have been elucidated by means of both analytical and spectroscopic methods. (C) 1998 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0014-827x(98)00090-1
  • 作为产物:
    描述:
    1-(4-methylphenyl)-3-carbethoxy-4,5,6,7-tetrahydroindazolesodium hydroxide 作用下, 以 乙醇 为溶剂, 以90%的产率得到1-(4-methylphenyl)-4,5,6,7-tetrahydroindazole-3-carboxylic acid
    参考文献:
    名称:
    New cycloalkylpyrazoles as potential cyclooxygenase inhibitors
    摘要:
    In this study some cycloalkyl-3-(N-substituted carbamoyl)-1-phenylpyrazoles have been synthesized in order to screen their capability to inhibit human cyclooxygenase. The synthetic pathway is based on the well known property of nitrilimines to undergo 1,3-dipolar cycloaddition reactions. The structures of all the synthesized compounds have been elucidated by means of both analytical and spectroscopic methods. (C) 1998 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0014-827x(98)00090-1
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