6-methylcyclohexa-2,4-dienone | 74428-28-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 6-methylcyclohexa-2,4-dienone
• 英文别名: 6-Methylcyclohexa-2,4-dien-1-one
• CAS: 74428-28-7
• 化学式: C₇H₈O
• 分子量: 108.14
• InChiKey: JQGQIRPONOJDCO-UHFFFAOYSA-N

物化性质

• 沸点：
  187.3±10.0 °C(Predicted)
• 密度：
  0.987±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  8
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  3-Methyl-bicyclo<2.2.2>oct-5-en-2-on 800.0 ℃ 、0.01 Pa 条件下， 生成 乙烯 、 6-methylcyclohexa-2,4-dienone 、 苯酚
  参考文献：
  名称：

  逆向反应-X顺式-反-阿尔德-乙二酮互变异构体-苯酚的反应。

  摘要：

  DOI：

  10.1016/s0040-4039(00)71433-x

文献信息

• Fused Imidazo [3,2 - D] Pyrazines as P13 Kinase Inhibitors
  申请人：Pastor Fernández Joaquin

  公开号：US20130029967A1

  公开（公告）日：2013-01-31

  There is provided compounds of formula (I), wherein A 1 , A 2 , A 3 , A 4 , n, the dotted lines, B 1 , B 1a , B 2 , B 2a , B 3 , B 3a , B 4 , B 4a , R 2 and R 3 have meanings given in the description, and pharmaceutically-acceptable esters, amides, solvates or salts thereof, which compounds are useful in the treatment of diseases in which inhibition of a protein kinase (e.g. a PI3-K and/or mTOR) is desired and/or required, and particularly in the treatment of cancer or a proliferative disease.

  提供了式（I）的化合物，其中A1，A2，A3，A4，n，点线，B1，B1a，B2，B2a，B3，B3a，B4，B4a，R2和R3的含义在说明中给出，并且其药学上可接受的酯，酰胺，溶剂合物或盐，这些化合物在治疗需要抑制蛋白激酶（例如PI3-K和/或mTOR）的疾病中非常有用，特别是在治疗癌症或增生性疾病方面。
• Modulation of Pathogenicity
  申请人：Ammendola Aldo

  公开号：US20070197492A1

  公开（公告）日：2007-08-23

  The present invention relates to the use of compounds of the general Formula (XIII): In particular the invention refers to a family of compounds that block the quorum sensing system of Gram-negative bacteria, a process for their manufacture, pharmaceutical compositions containing them and to their use for the treatment and prevention of microbial damages and diseases, in particular for diseases where there is an advantage in inhibiting quorum sensing regulated phenotypes of pathogens.
• Modulation of pathogcnicity
  申请人：Ammendola Aldo

  公开号：US20080194588A1

  公开（公告）日：2008-08-14

  The present invention relates to the use of compounds of the general Formula (I): wherein in Formula (I), R is H, alkyl, cycloalkyl, aryl or heteroaryl; R 1 is H, alkyl, cycloalkyl, aryl or heteroaryl; R 2 is H, alkyl, cycloalkyl, aryl or heteroaryl; A 1 and A 2 each independently represent an optionally substituted C 1 -C 20 -alkyl group which may contain one or more group(s) Z, or a monocyclic or polycyclic optionally substituted aromatic or non-aromatic ring system which may contain one or more group(s) X, and in case of a polycyclic ring system, said system contains at least one aromatic ring; Z is selected from the group consisting of S, O, N, NR 4 , CO, CO 2 , CS, SO or SO 2 X is selected from the group consisting of S, O, N, NR 4 , SO or SO 2 ;
• Modulation of pathogenicity
  申请人：Ammendola Aldo

  公开号：US20080176938A1

  公开（公告）日：2008-07-24

  The present invention relates to the use of compounds of the general Formula (1): wherein in Formula (1), R is H, alkyl, cycloalkyl, aryl or heteroaryl; R 1 is H, alkyl, cycloalkyl, aryl or heteroaryl; R 2 is H, alkyl, cycloalkyl, aryl or heteroaryl; A 1 and A 2 each independently represent an optionally substituted C 1 -C 20 -alkyl group which may contain one or more group(s) Z, or a monocyclic or polycyclic optionally substituted aromatic or non-aromatic ring system which may contain one or more group(s) X, and in case of a polycyclic ring system, said system contains at least one aromatic ring; Z is selected from the group consisting of S, O, N, NR 4 , CO, CO 2 , CS, SO or SO 2 X is selected from the group consisting of S, O, N, NR 4 , SO or SO 2 .
• US3996169A
  申请人：——

  公开号：US3996169A

  公开（公告）日：1976-12-07