1-o-tolylcyclobutanecarbonitrile | 29786-39-8

• 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: 1-o-tolylcyclobutanecarbonitrile
• 英文别名: 1-(o-tolyl)cyclobutane-1-carbonitrile；1-o-Tolylcyclobutancarbonitril；1-(2-Methylphenyl)cyclobutanecarbonitrile；1-(2-methylphenyl)cyclobutane-1-carbonitrile
• CAS: 29786-39-8
• 化学式: C₁₂H₁₃N
• 分子量: 171.242
• InChiKey: JKJIAVWVTFWKPR-UHFFFAOYSA-N

物化性质

• 沸点：
  305.6±21.0 °C(Predicted)
• 密度：
  1.04±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  23.8
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  1-o-tolylcyclobutanecarbonitrile 在 sodium hydroxide 、 双氧水 作用下， 生成 <(1-o-Tolylcyclobutyl)carbonyl>carbamsaeuremethylester
  参考文献：
  名称：

  (1-arylcyclobutyl)carbonyl carbamic acid derivatives

  摘要：

  公开号：

  US03526656A1
• 作为产物：
  描述：

  1,3-二溴丙烷 、 邻甲基苯乙腈 在 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 4.0h， 以22.4%的产率得到1-o-tolylcyclobutanecarbonitrile
  参考文献：
  名称：

  KR2017/43091

  摘要：

  公开号：

文献信息

• [EN] NOVEL TRPV3 MODULATORS<br/>[FR] NOUVEAUX MODULATEURS DE TRPV3
  申请人：ABBOTT LAB

  公开号：WO2012019315A1

  公开（公告）日：2012-02-16

  Disclosed herein are modulators of TRPV3 of formula (I), wherein G1, X1, X2, X3, X4, X5, G2, Z1, Ra, Rb, u, and p are as defined in the specification. Compositions comprising such compounds and methods for treating conditions and disorders using such compounds and compositions are also presented.

  本文公开了式（I）的TRPV3调节剂，其中G1、X1、X2、X3、X4、X5、G2、Z1、Ra、Rb、u和p的定义如规范中所述。还提供了包含这些化合物的组合物以及使用这些化合物和组合物治疗疾病和疾病的方法。
• NOVEL TRPV3 MODULATORS
  申请人：AbbVie Inc.

  公开号：US20130150409A1

  公开（公告）日：2013-06-13

  Disclosed herein are modulators of TRPV3 of formula (I) wherein G 1 , X 1 , X 2 , X 3 , X 4 , X 5 , G 2 , Z 1 , R a , R b , u, and p are as defined in the specification. Compositions comprising such compounds and methods for treating conditions and disorders using such compounds and compositions are also presented.

  本文披露了具有以下结构的TRPV3调节剂（I）其中G1、X1、X2、X3、X4、X5、G2、Z1、Ra、Rb、u和p如规范中所定义。还提供了包含这种化合物的组合物以及使用这种化合物和组合物治疗疾病和疾病的方法。
• OXADIAZOLE AMINE DERIVATIVE COMPOUNDS AS HISTONE DEACETYLASE 6 INHIBITOR, AND THE PHARMACEUTICAL COMPOSITION COMPRISING THE SAME
  申请人：Chong Kun Dang Pharmaceutical Corp.

  公开号：EP3362445A1

  公开（公告）日：2018-08-22
• US9156788B2
  申请人：——

  公开号：US9156788B2

  公开（公告）日：2015-10-13
• [EN] OXADIAZOLE AMINE DERIVATIVE COMPOUNDS AS HISTONE DEACETYLASE 6 INHIBITOR, AND THE PHARMACEUTICAL COMPOSITION COMPRISING THE SAME<br/>[FR] COMPOSÉS DÉRIVÉS D'OXADIAZOLE AMINE UTILISÉS EN TANT QU'INHIBITEUR DE L'HISTONE DÉSACÉTYLASE 6, ET COMPOSITION PHARMACEUTIQUE LES COMPRENANT
  申请人：CHONG KUN DANG PHARMACEUTICAL CORP

  公开号：WO2017065473A1

  公开（公告）日：2017-04-20

  The present disclosure relates to novel compounds having histone deacetylase 6 (HDAC6) inhibitory activity, stereoisomers thereof or pharmaceutically acceptable salts thereof, the use thereof for the preparation of therapeutic medicaments, pharmaceutical compositions containing the same, a method for treating diseases using the composition, and methods for preparing the novel compounds. The novel compounds, stereoisomers thereof or pharmaceutically acceptable salts thereof according to the present disclosure have histone deacetylase (HDAC) inhibitory activity and are effective for the prevention or treatment of HDAC6-mediated diseases, including infectious diseases; neoplasms; endocrine, nutritional and metabolic diseases; mental and behavioral disorders; neurological diseases; diseases of the eye and adnexa; cardiovascular diseases; respiratory diseases; digestive diseases; diseases of the skin and subcutaneous tissue; diseases of the musculoskeletal system and connective tissue; or congenital malformations, deformations and chromosomal abnormalities.