ethyl 3-(2-cyanophenyl)-1H-indene-2-carboxylate

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 肉桂酸及其衍生物
• 英文名称: ethyl 3-(2-cyanophenyl)-1H-indene-2-carboxylate
• 化学式: C₁₉H₁₅NO₂
• 分子量: 289.3
• InChiKey: YUPXZQCBUBZUHW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  22
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.16
• 拓扑面积：
  50.1
• 氢给体数：
  0
• 氢受体数：
  3

文献信息

• [EN] PROCESS TO MAKE HIGHLY SUBSTITUTED INDENES USING METAL SLAT CATALYSTS<br/>[FR] PROCÉDÉ DE PRODUCTION D'INDÈNES FORTEMENT SUBSTITUÉS À L'AIDE DE CATALYSEURS DE TYPE SEL MÉTALLIQUE
  申请人：ROSOCHA GREGORY

  公开号：WO2014064477A1

  公开（公告）日：2014-05-01

  The present invention is a process to make l-aryl-2-bromo substituted indenes and l-phenyl-2-bromo substituted indenes that can have different functional groups present around the indene ring and/or the aromatic and/or phenyl ring. The indenes are made using the corresponding 1,2- biaryl-gem-dibromocyclopropane and/or 1,2-biphenyl-gem-dibromocyclopropanes and/or 1-aryl- 2-phenyl-gem-dibromocyclopropanes using a metal salts, a solvent, low temperatures.

  本发明是一种制备具有不同官能团的1-芳基-2-溴代茚和1-苯基-2-溴代茚的过程，这些官能团可以存在于茚环和/或芳香环和/或苯环周围。使用相应的1,2-双芳基-双溴环丙烷和/或1,2-双苯基-双溴环丙烷和/或1-芳基-2-苯基-双溴环丙烷，利用金属盐、溶剂和低温制备茚烯。
• PROCESS TO MAKE HIGHLY SUBSTITUTED INDENES USING METAL SLAT CATALYSTS
  申请人：ROSOCHA Gregory

  公开号：US20150274617A1

  公开（公告）日：2015-10-01

  The present invention is a process to make 1-aryl-2-bromo substituted indenes and 1-phenyl-2-bromo substituted indenes that can have different functional groups present around the indene ring and/or the aromatic and/or phenyl ring. The indenes are made using the corresponding 1,2-biaryl-gem-dibromocyclopropane and/or 1,2-biphenyl-gem-dibromocyclopropanes and/or 1-aryl-2-phenyl-gem-dibromocyclopropanes using a metal salts, a solvent, low temperatures.
• THE SYNTHESIS OF TETRAHYDROISOQUINOLINES FROM 2-METHYL-1-PHENYL SUBSTITUTED INDENES
  申请人：ROSOCHA Gregory

  公开号：US20150284332A1

  公开（公告）日：2015-10-08

  A procedure for the synthesis of tetrahydroisoquinolines from 2-methyl-1-phenyl substituted indene is described. The process involves the use of osmium tetroxide to cleave the indene double bond forming the keto aldehyde product, which is then combined with a substituted amine forming the substituted isoquinoline. Isoquinolines can be useful as industrial products in the chemical, agrochemical, oil and gas industry, as well as useful as medicaments in the pharmaceutical industry.