1-acetyl-5-methyl-5-thiophen-2-yl-imidazolidine-2,4-dione | 62031-98-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑烷类
• 英文名称: 1-acetyl-5-methyl-5-thiophen-2-yl-imidazolidine-2,4-dione
• 英文别名: 1-Acetyl-5-methyl-5-thiophen-2-ylimidazolidine-2,4-dione
• CAS: 62031-98-5
• 化学式: C₁₀H₁₀N₂O₃S
• 分子量: 238.267
• InChiKey: VPHKWGXQYUXANR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.5
• 重原子数：
  16
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  94.7
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  1-acetyl-5-methyl-5-thiophen-2-yl-imidazolidine-2,4-dione 在 氯 、 sodium carbonate 作用下， 生成 1-acetyl-3-chloro-5-methyl-5-thiophen-2-yl-imidazolidine-2,4-dione
  参考文献：
  名称：

  Hydantoins as antitumor agents

  摘要：

  A series of 27 hydantoins was prepared and tested as antitumor agents. These were variously substituted in the 5 position but with special emphasis on the substituents (chloro, acetyl, chloroacetyl, and methyl) in the 1 and/or 3 positions. The most active compound was 5,5-bis(4-chlorophenyl)-1,3-dichlorohydantoin with a T/C value of 190% against P-388 lymphocytic leukemia in mice.

  DOI：

  10.1021/jm00214a031
• 作为产物：
  描述：

  5-甲基-5-噻吩-2-咪唑烷-2,4-二酮 、 乙酰氯 在 吡啶 作用下， 生成 1-acetyl-5-methyl-5-thiophen-2-yl-imidazolidine-2,4-dione
  参考文献：
  名称：

  Hydantoins as antitumor agents

  摘要：

  A series of 27 hydantoins was prepared and tested as antitumor agents. These were variously substituted in the 5 position but with special emphasis on the substituents (chloro, acetyl, chloroacetyl, and methyl) in the 1 and/or 3 positions. The most active compound was 5,5-bis(4-chlorophenyl)-1,3-dichlorohydantoin with a T/C value of 190% against P-388 lymphocytic leukemia in mice.

  DOI：

  10.1021/jm00214a031

文献信息

• Hydantoins as antitumor agents
  作者：Thomas R. Rodgers、Maurice P. LaMontagne、Anica Markovac、Arthur B. Ash

  DOI：10.1021/jm00214a031

  日期：1977.4

  A series of 27 hydantoins was prepared and tested as antitumor agents. These were variously substituted in the 5 position but with special emphasis on the substituents (chloro, acetyl, chloroacetyl, and methyl) in the 1 and/or 3 positions. The most active compound was 5,5-bis(4-chlorophenyl)-1,3-dichlorohydantoin with a T/C value of 190% against P-388 lymphocytic leukemia in mice.