1H-吡唑,1-乙酰基-4,5-二氢-3-(7-羟基-4-甲基-2-羰基-2H-1-苯并吡喃-8-基)-5-(2-羟基苯基)- | 139640-51-0

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 香豆素及其衍生物
• 中文名称: 1H-吡唑,1-乙酰基-4,5-二氢-3-(7-羟基-4-甲基-2-羰基-2H-1-苯并吡喃-8-基)-5-(2-羟基苯基)-
• 英文名称: 8-(1-acetyl-4,5-dihydro-5-(2-hydroxyphenyl)-1H-pyrazol-3-yl)-7-hydroxy-4-methyl-2H-1-benzopyran-2-one
• 英文别名: 8-[2-Acetyl-3-(2-hydroxyphenyl)-3,4-dihydropyrazol-5-yl]-7-hydroxy-4-methylchromen-2-one；8-[2-acetyl-3-(2-hydroxyphenyl)-3,4-dihydropyrazol-5-yl]-7-hydroxy-4-methylchromen-2-one
• CAS: 139640-51-0
• 化学式: C₂₁H₁₈N₂O₅
• 分子量: 378.384
• InChiKey: FZGQCKZLWZZMAW-UHFFFAOYSA-N

物化性质

• 沸点：
  583.5±60.0 °C(Predicted)
• 密度：
  1.42±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  28
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  99.4
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  8-乙酰基-7-羟基-4-甲基-2H-1-苯并吡喃-2-酮 在 哌啶 、 一水合肼 作用下， 以 乙醇 、 苯 为溶剂， 反应 12.5h， 生成 1H-吡唑,1-乙酰基-4,5-二氢-3-(7-羟基-4-甲基-2-羰基-2H-1-苯并吡喃-8-基)-5-(2-羟基苯基)-
  参考文献：
  名称：

  Bhalla, Manish; Naithani, P K; Kumar, A, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1992, vol. 31, # 3, p. 183 - 186

  摘要：

  DOI：

文献信息

• Bhalla, Manish; Naithani, P K; Kumar, A, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1992, vol. 31, # 3, p. 183 - 186
  作者：Bhalla, Manish、Naithani, P K、Kumar, A、Bhalla, T N、Shanker, K

  DOI：——

  日期：——
• Synthesis of 4-methylcoumarin derivatives containing 4,5-dihydropyrazole moiety to scavenge radicals and to protect DNA
  作者：Chuan Xiao、Xu-Yang Luo、De-Jun Li、Hang Lu、Zai-Qun Liu、Zhi-Guang Song、Ying-Hua Jin

  DOI：10.1016/j.ejmech.2012.03.052

  日期：2012.7

  A series of 4-methylcoumarin derivatives containing 4,5-dihydropyrazole moiety were synthesized and their antioxidant activities were evaluated in AAPH (2,2'-azobis(2-amidinopropane hydrochloride))-induced oxidation of DNA, and in trapping DPPH (2,2'-diphenyl-1-picrylhydrazyl) and ABTS(+center dot) (2,2'-azinobis(3-ethylbenzothiazoline-6-sulfonate) cationic radical), respectively. Among coumarin derivatives, 3a-d and 4a-c exhibited the termination of radical propagation-chains in AAPH-induced oxidation of DNA. The ortho dihydroxyphenyl substitution at 5 position and 1-unsubstitution of the 4,5-dihydroxylpyrazole was found enhancing the antioxidant activities of these coumarin derivatives. (C) 2012 Elsevier Masson SAS. All rights reserved.