2-Benzylcycloheptanol | 55166-20-6

• 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-Benzylcycloheptanol
• 英文别名: 2-Benzylcycloheptan-1-ol
• CAS: 55166-20-6；55166-21-7
• 化学式: C₁₄H₂₀O
• 分子量: 204.312
• InChiKey: FLOGZIUYUSDYEM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  2-benzylidene-cycloheptanone 在 palladium on activated charcoal 氢气 作用下， 以 四氢呋喃 为溶剂， 反应 24.0h， 生成 2-Benzylcycloheptanol 、 2-benzylcycloheptan-1-one
  参考文献：
  名称：

  Synthesis of certain unsubstituted, 9-exo-(dialkylaminomethyl)-, and 9-endo-(aralkyl)-tricyclo[5.2.1.02,6]decane-8-ketoxime esters and ethers with local anesthetic and analgesic activities

  摘要：

  The synthesis of series of unsubstituted, 9-exo-(dialkylaminomethyl)-, and 9-endo-(aralkyl)tricyclo [5.2.1.0(2,6)]decane-8-ketoximes esters and ethers 3a-j, 3a-d, 7a-j and 13a-d from the oxime synthons 2, 6a-e, 12a and 12b, respectively, is described. All the obtained compounds displayed noticeable local anesthetic potential. Among them, the oximino ether 4d (ED50 = 0.15 mg/kg) and the oximino ester 3a (ED50 = 0.23 mg/kg) are the most active of the series and possess higher potential than the reference standards. Some of the target compounds evoked analgesic effect, specially the oximino ether 7i which is the most potent of the series and is stronger than acetylsalicylic acid but weaker than morphine hydrochloride. (C) 1998 Elsevier Science S.A. All rights reserved.

  DOI：

  10.1016/s0014-827x(98)00008-1

文献信息

• US4117164A
  申请人：——

  公开号：US4117164A

  公开（公告）日：1978-09-26
• Synthesis of certain unsubstituted, 9-exo-(dialkylaminomethyl)-, and 9-endo-(aralkyl)-tricyclo[5.2.1.02,6]decane-8-ketoxime esters and ethers with local anesthetic and analgesic activities
  作者：M.Nabil Aboul-Enein、Aida El-Azzouny、Nevine A. Abdallah、Yousreya A. Maklad、Ola A. Saleh、M.Y. Ebeid

  DOI：10.1016/s0014-827x(98)00008-1

  日期：1998.3

  The synthesis of series of unsubstituted, 9-exo-(dialkylaminomethyl)-, and 9-endo-(aralkyl)tricyclo [5.2.1.0(2,6)]decane-8-ketoximes esters and ethers 3a-j, 3a-d, 7a-j and 13a-d from the oxime synthons 2, 6a-e, 12a and 12b, respectively, is described. All the obtained compounds displayed noticeable local anesthetic potential. Among them, the oximino ether 4d (ED50 = 0.15 mg/kg) and the oximino ester 3a (ED50 = 0.23 mg/kg) are the most active of the series and possess higher potential than the reference standards. Some of the target compounds evoked analgesic effect, specially the oximino ether 7i which is the most potent of the series and is stronger than acetylsalicylic acid but weaker than morphine hydrochloride. (C) 1998 Elsevier Science S.A. All rights reserved.