2-(chloroseleno)benzenesulfonyl chloride | 199605-37-3

• 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: 2-(chloroseleno)benzenesulfonyl chloride
• 英文别名: (2-Chlorosulfonylphenyl) selenohypochlorite
• CAS: 199605-37-3
• 化学式: C₆H₄Cl₂O₂SSe
• 分子量: 290.029
• InChiKey: HWYNVEFOXHYJJG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  42.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-(chloroseleno)benzenesulfonyl chloride 生成 双(2-氯磺酰基苯基)二硒化物
  参考文献：
  名称：

  Bis(2-Chlorosulfonylphenyl) Diselenide—the Substrate for Organoselenium Sulfonamides

  摘要：

  Synthesis of bis(2-chlorosulfonylphenyl) diselenide (11) from 2-aminobenzenesulfonic acid was elaborated. It was shown that (11) is a good starting material for synthesis of the organoselenium sulfonamides, such as bis(2-sulfamoylphenyl) diselenides (3)and benz-2,3-azaselenathiophene I,l-dioxides (4), being potential immunostimulants and oxidation catalysts.

  DOI：

  10.1080/00397919708005450
• 作为产物：
  描述：

  2-sulfo-benzenediazonium-betaine 在 五氯化磷 作用下， 以 水 为溶剂， 反应 14.0h， 生成 2-(chloroseleno)benzenesulfonyl chloride
  参考文献：
  名称：

  Bis(2-Chlorosulfonylphenyl) Diselenide—the Substrate for Organoselenium Sulfonamides

  摘要：

  Synthesis of bis(2-chlorosulfonylphenyl) diselenide (11) from 2-aminobenzenesulfonic acid was elaborated. It was shown that (11) is a good starting material for synthesis of the organoselenium sulfonamides, such as bis(2-sulfamoylphenyl) diselenides (3)and benz-2,3-azaselenathiophene I,l-dioxides (4), being potential immunostimulants and oxidation catalysts.

  DOI：

  10.1080/00397919708005450

文献信息

• Bis(2-Chlorosulfonylphenyl) Diselenide—the Substrate for Organoselenium Sulfonamides
  作者：Krystian Kloc、Jacek Mlochowski、Sungano Mhizha

  DOI：10.1080/00397919708005450

  日期：1997.12

  Synthesis of bis(2-chlorosulfonylphenyl) diselenide (11) from 2-aminobenzenesulfonic acid was elaborated. It was shown that (11) is a good starting material for synthesis of the organoselenium sulfonamides, such as bis(2-sulfamoylphenyl) diselenides (3)and benz-2,3-azaselenathiophene I,l-dioxides (4), being potential immunostimulants and oxidation catalysts.