3-Isothiocyanato-4'-methoxy-2-methyl-biphenyl | 546094-38-6

• 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: 3-Isothiocyanato-4'-methoxy-2-methyl-biphenyl
• 英文别名: 1-Isothiocyanato-3-(4-methoxyphenyl)-2-methylbenzene
• CAS: 546094-38-6
• 化学式: C₁₅H₁₃NOS
• 分子量: 255.34
• InChiKey: PJSXBBYCPHCLAZ-UHFFFAOYSA-N

物化性质

• 沸点：
  406.6±45.0 °C(Predicted)
• 密度：
  1.08±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.3
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.13
• 拓扑面积：
  53.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-Isothiocyanato-4'-methoxy-2-methyl-biphenyl 在 mercury(II) oxide 作用下， 以 乙醇 、 二氯甲烷 为溶剂， 反应 26.0h， 生成 N-[3-(4-methoxyphenyl)-2-methylphenyl]-4,5-dihydro-1H-imidazol-2-amine
  参考文献：
  名称：

  Discovery of a series of (4,5-Dihydroimidazol-2-yl)-biphenylamine 5-HT7 agonists

  摘要：

  A novel (4,5-dihydroimidazol-2-yl)-biphenylamine series of 5-HT7 agonist compounds was developed from a structurally related lead compound 1. The newly discovered series is exemplified by compound 2 that possesses high affinity for 5-HT7 receptors and shows intrinsic agonist activity in functional assays. This new series has significant alpha(1) and alpha(2) activities perhaps due to the presence of the 2-aminoimidazoline moiety. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00925-3
• 作为产物：
  描述：

  4a(2)-Methoxy-2-methyl-3-nitro-1,1a(2)-biphenyl 在 盐酸 、 乙胺嗪 、 铁粉 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 反应 26.0h， 生成 3-Isothiocyanato-4'-methoxy-2-methyl-biphenyl
  参考文献：
  名称：

  Discovery of a series of (4,5-Dihydroimidazol-2-yl)-biphenylamine 5-HT7 agonists

  摘要：

  A novel (4,5-dihydroimidazol-2-yl)-biphenylamine series of 5-HT7 agonist compounds was developed from a structurally related lead compound 1. The newly discovered series is exemplified by compound 2 that possesses high affinity for 5-HT7 receptors and shows intrinsic agonist activity in functional assays. This new series has significant alpha(1) and alpha(2) activities perhaps due to the presence of the 2-aminoimidazoline moiety. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00925-3