1-[3-methyl-2-(2-chlorophenyldiazenyl)-2H-aziren-2-yl]ethanone | 1398415-35-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 1-[3-methyl-2-(2-chlorophenyldiazenyl)-2H-aziren-2-yl]ethanone
• 英文别名: 1-[2-[(2-Chlorophenyl)diazenyl]-3-methylazirin-2-yl]ethanone；1-[2-[(2-chlorophenyl)diazenyl]-3-methylazirin-2-yl]ethanone
• CAS: 1398415-35-4
• 化学式: C₁₁H₁₀ClN₃O
• 分子量: 235.673
• InChiKey: NLTLJRJMBXVWHA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  54.2
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  pentane-2,3,4-trione 3-[(2-chloro-phenyl)-hydrazone] 在 盐酸羟胺 、 sodium acetate 、 potassium hydroxide 作用下， 以 水 为溶剂， 反应 6.5h， 生成 1-[3-methyl-2-(2-chlorophenyldiazenyl)-2H-aziren-2-yl]ethanone
  参考文献：
  名称：

  Synthesis and QSAR modeling 1-[3-methyl-2-(aryldiazenyl)-2H-aziren-2-yl]ethanones as potential antibacterial agents

  摘要：

  The present communication deals with the synthesis of a series of 1-[3-methyl-2-(aryldiazenyl)-2H-aziren-2-yl]ethanones. The compounds were synthesized in excellent yields (70-80 %), and the structures were established on the basis of consistent IR, H-1 NMR, and elemental analysis data. The purity has been ascertained by chromatographic resolution using hexane-ethyl acetate (6:4 v/v) as binary eluent. All the compounds have been tested for their antimicrobial activity against a representative panel of bacteria i.e., Bacillus subtilis, Escherichia coli, Pseudomonas diminuta, and Staphylococcus aureus using Chloramphenicol as reference drug. All the synthesized compounds were found to exhibit profound antimicrobial activity.

  DOI：

  10.1007/s00044-012-0242-4

文献信息

• Synthesis and QSAR modeling 1-[3-methyl-2-(aryldiazenyl)-2H-aziren-2-yl]ethanones as potential antibacterial agents
  作者：Vinita Sahu、Pratibha Sharma、Ashok Kumar

  DOI：10.1007/s00044-012-0242-4

  日期：2013.5

  The present communication deals with the synthesis of a series of 1-[3-methyl-2-(aryldiazenyl)-2H-aziren-2-yl]ethanones. The compounds were synthesized in excellent yields (70-80 %), and the structures were established on the basis of consistent IR, H-1 NMR, and elemental analysis data. The purity has been ascertained by chromatographic resolution using hexane-ethyl acetate (6:4 v/v) as binary eluent. All the compounds have been tested for their antimicrobial activity against a representative panel of bacteria i.e., Bacillus subtilis, Escherichia coli, Pseudomonas diminuta, and Staphylococcus aureus using Chloramphenicol as reference drug. All the synthesized compounds were found to exhibit profound antimicrobial activity.