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1-(3-methoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carbonyl chloride | 1159000-61-9

中文名称
——
中文别名
——
英文名称
1-(3-methoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carbonyl chloride
英文别名
——
1-(3-methoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carbonyl chloride化学式
CAS
1159000-61-9
化学式
C11H10ClN3O2
mdl
——
分子量
251.672
InChiKey
CODMPUPFHKKSBG-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

  • 熔点:
    125-126 °C
  • 沸点:
    417.6±55.0 °C(predicted)
  • 密度:
    1.36±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.96
  • 重原子数:
    17.0
  • 可旋转键数:
    3.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    57.01
  • 氢给体数:
    0.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    5-(2-甲基苯基)-1H-四唑1-(3-methoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carbonyl chloride吡啶 作用下, 反应 0.5h, 以62%的产率得到2-[1-(3-methoxyphenyl)-5-methyl-1H-1,2,3-triazol-4-yl]-5-(2-methylphenyl)-1,3,4-oxadiazole
    参考文献:
    名称:
    Synthesis of 1,2,4- and 1,3,4-oxadiazoles from 1-aryl-5-methyl-1H-1,2,3-triazole-4-carbonyl chlorides
    摘要:
    5-Substituted 2-(1-aryl-5-methyl-1H-1,2,3-triazol-4-yl)-1,3,4-oxadiazoles were synthesized by reaction of 1-aryl-5-methyl-1H-1,2,3-triazole-4-carbonyl chlorides with the corresponding 5-substituted 1H-tetrazoles. 5-Methyl-1-phenyl-1H-1,2,3-triazole-4-carbonyl chloride reacted with N'-hydroxybenzimidamides to give 3-aryl-5-(5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)-1,2,4-oxadiazoles. Reactions of 4-(5-methyl-1H-1,2,3-triazol-1-yl)benzoic acid with N'-hydroxybenzimidamides resulted in the formation of 3-aryl-5-[4-(5-methyl-1H-1,2,3-triazol-1-yl)phenyl]-1,2,4-oxadiazoles.
    DOI:
    10.1134/s1070428008100217
  • 作为产物:
    描述:
    5-methyl-1-[3-(methyloxy)phenyl]-1H-1,2,3-triazole-4-carboxylic acid氯化亚砜 作用下, 以 1,4-二氧六环 为溶剂, 以88%的产率得到1-(3-methoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carbonyl chloride
    参考文献:
    名称:
    Synthesis of 1,2,4- and 1,3,4-oxadiazoles from 1-aryl-5-methyl-1H-1,2,3-triazole-4-carbonyl chlorides
    摘要:
    5-Substituted 2-(1-aryl-5-methyl-1H-1,2,3-triazol-4-yl)-1,3,4-oxadiazoles were synthesized by reaction of 1-aryl-5-methyl-1H-1,2,3-triazole-4-carbonyl chlorides with the corresponding 5-substituted 1H-tetrazoles. 5-Methyl-1-phenyl-1H-1,2,3-triazole-4-carbonyl chloride reacted with N'-hydroxybenzimidamides to give 3-aryl-5-(5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)-1,2,4-oxadiazoles. Reactions of 4-(5-methyl-1H-1,2,3-triazol-1-yl)benzoic acid with N'-hydroxybenzimidamides resulted in the formation of 3-aryl-5-[4-(5-methyl-1H-1,2,3-triazol-1-yl)phenyl]-1,2,4-oxadiazoles.
    DOI:
    10.1134/s1070428008100217
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文献信息

  • Primary discovery of 1-aryl-5-substituted-1H-1,2,3-triazole-4-carboxamides as promising antimicrobial agents
    作者:Nazariy Pokhodylo、Nazar Manko、Nataliya Finiuk、Olha Klyuchivska、Vasyl Matiychuk、Mykola Obushak、Rostyslav Stoika
    DOI:10.1016/j.molstruc.2021.131146
    日期:2021.12
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