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1-(3-methylphenyl)-4-carboxy-5-methyl-1,2,3-triazole | 210159-14-1

中文名称
——
中文别名
——
英文名称
1-(3-methylphenyl)-4-carboxy-5-methyl-1,2,3-triazole
英文别名
5-methyl-1-(m-tolyl)-1H-1,2,3-triazole-4-carboxylic acid;5-methyl-1-(3-methylphenyl)-1H-1,2,3-triazole-4-carboxylic acid;5-methyl-1-(3-methylphenyl)triazole-4-carboxylic acid
1-(3-methylphenyl)-4-carboxy-5-methyl-1,2,3-triazole化学式
CAS
210159-14-1
化学式
C11H11N3O2
mdl
MFCD02168479
分子量
217.227
InChiKey
CFWWWVDWLUAXPU-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:
    158-159 °C(Solv: ethanol (64-17-5))
  • 沸点:
    448.7±47.0 °C(Predicted)
  • 密度:
    1.31±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.181
  • 拓扑面积:
    68
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Triazole-Based Inhibitors of the Wnt/β-Catenin Signaling Pathway Improve Glucose and Lipid Metabolisms in Diet-Induced Obese Mice
    作者:Obinna N. Obianom、Yong Ai、Yingjun Li、Wei Yang、Dong Guo、Hong Yang、Srilatha Sakamuru、Menghang Xia、Fengtian Xue、Yan Shu
    DOI:10.1021/acs.jmedchem.8b01408
    日期:2019.1.24
    implicated in the etiology and progression of metabolic disorders. Although lines of genetic evidence suggest that blockage of this pathway yields favorable outcomes in treating such ailments, few inhibitors have been used to validate the promising genetic findings. Here, we synthesized and characterized a novel class of triazole-based Wnt/β-catenin signaling inhibitors and assessed their effects on energy
    Wnt /β-catenin信号传导途径与代谢紊乱的病因和进展有关。尽管遗传证据表明该途径的阻断在治疗此类疾病方面产生了有利的结果,但很少有抑制剂被用于验证有前途的遗传发现。在这里,我们合成和表征了一类新型的基于三唑的Wnt /β-catenin信号抑制剂,并评估了它们对能量代谢的影响。最重要的抑制剂之一化合物3a促进了Axin的稳定,从而导致蛋白酶体降解β-catenin,并随后抑制了细胞中Wnt /β-catenin的信号传导。用化合物3a处理肝细胞和高脂饮食喂养的小鼠导致肝脂质蓄积明显减少。而且,化合物3a改善了高脂饮食喂养小鼠的葡萄糖耐量,而没有明显的毒性,同时下调了参与葡萄糖脂肪酸代谢的基因。预期将进一步开发新的抑制剂来治疗代谢紊乱。
  • Synthesis of 1,2,4- and 1,3,4-oxadiazoles from 1-aryl-5-methyl-1H-1,2,3-triazole-4-carbonyl chlorides
    作者:N. D. Obushak、N. T. Pokhodylo、N. I. Pidlypnyi、V. S. Matiichuk
    DOI:10.1134/s1070428008100217
    日期:2008.10
    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.
  • Chu; Sun; Zhang, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2001, vol. 40, # 9, p. 854 - 856
    作者:Chu、Sun、Zhang、Li、Liao
    DOI:——
    日期:——
  • Studies on Condensed Heterocyclic Compounds XVII. Synthesis of 6-(1-Aryl-5-methyl-1,2,3-triazol-4-yl)-3-phenyl-s-triazolo[3,4-<i>b</i>]-1,3,4-thiadiazoles
    作者:Xiao-Wen Sun、Yan Zhang、Zi-Yi Zhang
    DOI:10.1002/jccs.199800080
    日期:1998.8
    AbstractTreatment of 4‐amino‐5‐mercapto‐3‐phenyl‐1,2,4‐triazole 2 with 1‐aryl‐4‐carboxy‐5‐methyl‐1,2,3‐triazoles 1a‐1j in a one‐step reaction yielded several 6‐(1‐aryl‐5‐methyl‐1,2,3‐triazol‐4‐yl)‐3‐phenyl‐s‐triazolo[3,4‐b]‐1,3,4‐thiadiazoles 3a‐3j. The structures of all the products were established on the basis of elemental analyses and spectral data. The fragmentation of the mass spectra of 3a‐3j under electron impact was discussed.
  • Sun, Xiao-Wen; Zhang, Yan; Zhang, Zi-Yi, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1999, vol. 38, # 3, p. 380 - 383
    作者:Sun, Xiao-Wen、Zhang, Yan、Zhang, Zi-Yi、Wang, Qin、Wang, Shu-Fang
    DOI:——
    日期:——
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