(4-methyl-[1]naphthyl)-[1]naphthyl ketone | 873963-22-5

• 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: (4-methyl-[1]naphthyl)-[1]naphthyl ketone
• 英文别名: (4-Methyl-[1]naphthyl)-[1]naphthyl-keton；(4-Methylnaphthalen-1-yl)-naphthalen-1-ylmethanone
• CAS: 873963-22-5
• 化学式: C₂₂H₁₆O
• 分子量: 296.368
• InChiKey: KVMCBBNMOSUVHL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.1
• 重原子数：
  23
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.05
• 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：

  氰基萘 、 alkaline earth salt of/the/ methylsulfuric acid 生成 (4-methyl-[1]naphthyl)-[1]naphthyl ketone
  参考文献：
  名称：

  105.多环芳烃。第十七部分。完成十二种单甲基-1：2-苯并蒽的合成

  摘要：

  DOI：

  10.1039/jr9380000505

文献信息

• 149. Oxidative ring closure in the Friedel–Crafts reaction. Part II. Condensation of aromatic acid chlorides with naphthalene derivatives
  作者：Gerard D. Buckley

  DOI：10.1039/jr9450000564

  日期：——
• Combinations for treating HIV-associated pain
  申请人：Johns Donald

  公开号：US20090281194A1

  公开（公告）日：2009-11-12

  The present invention relates to novel combinations suitable for the treatment or amelioration of pain of various genesis or aetiology, which comprise, as active ingredients, at least one cannabinoid receptor binding compound, in particular a cannabinoid receptor binding naphthalene derivative, and at least one opioid, to their preparation, to their use as medicaments and to medicaments comprising them.
• 105. Polycyclic aromatic hydrocarbons. Part XVII. Completion of the synthesis of the twelve monomethyl-1 : 2-benzanthracenes
  作者：J. W. Cook、A. M. Robinson

  DOI：10.1039/jr9380000505

  日期：——