Di(4-cyclopropylphenyl)disulfid | 54997-87-4

• 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: Di(4-cyclopropylphenyl)disulfid
• 英文别名: 1-Cyclopropyl-4-[(4-cyclopropylphenyl)disulfanyl]benzene；1-cyclopropyl-4-[(4-cyclopropylphenyl)disulfanyl]benzene
• CAS: 54997-87-4
• 化学式: C₁₈H₁₈S₂
• 分子量: 298.473
• InChiKey: YAZDPZPKBBEZLR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.8
• 重原子数：
  20
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  50.6
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  4-溴环丙基苯 在 sodium hydroxide 、 双氧水 作用下， 生成 Di(4-cyclopropylphenyl)disulfid
  参考文献：
  名称：

  8-Alkyl and 8-cycloalkyl-10-piperazinodibenzo[b,f]thiepins

  摘要：

  DOI：

  10.1135/cccc19740783

文献信息

• PROCESS FOR PRODUCING ARYLSULFUR PENTAFLUORIDES
  申请人：UMEMOTO TERUO

  公开号：US20080234520A1

  公开（公告）日：2008-09-25

  Novel processes for preparing arylsulfur pentafluorides are disclosed. Processes include reacting at least one aryl sulfur compound with a halogen and a fluoro salt to form an arylsulfur halotetrafluoride. The arylsulfur halotetrafluoride is reacted with a fluoride source to form a target arylsulfur pentafluoride.

  揭示了制备芳基硫五氟化物的新工艺。该工艺包括将至少一种芳基硫化合物与卤素和氟盐反应，形成芳基硫卤四氟化物。然后将芳基硫卤四氟化物与氟化物源反应，形成目标芳基硫五氟化物。
• Process for producing arylsulfur halotetrafluorides
  申请人：UBE Industries, Ltd.

  公开号：EP2468722A1

  公开（公告）日：2012-06-27

  Novel processes for preparing arylsulfur pentafluorides are disclosed. Processes include reacting at least one aryl sulfur compound with a halogen and a fluoro salt to form an arylsufur halotetrafluoride. The arylsulfur halotetrafluoride is reacted with a fluoride source to form a target arylsulfur pentafluoride.

  本发明公开了制备芳基五氟化硫的新工艺。该工艺包括将至少一种芳基硫化合物与卤素和氟盐反应生成芳基硫卤四氟化物。该芳基四氟化硫与氟化源反应生成目标芳基五氟化硫。
• Process for producing arylsulfur pentafluorides
  申请人：UBE Industries, Ltd.

  公开号：EP2468719B1

  公开（公告）日：2013-10-16
• EP2468722B1
  申请人：——

  公开号：EP2468722B1

  公开（公告）日：2014-10-01
• Process for Producing Arylsulfur Pentafluorides
  申请人：Umemoto Teruo

  公开号：US20090287024A1

  公开（公告）日：2009-11-19

  Novel processes for preparing arylsulfur pentafluorides are disclosed. Processes include reacting at least one aryl sulfur compound with a halogen and a fluoro salt to form an arylsulfur halotetrafluoride. The arylsulfur halotetrafluoride is reacted with a fluoride source to form a target arylsulfur pentafluoride.