4-Chloro-1-methoxy-2-(3-methoxyphenyl)benzene | 565203-84-1

• 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-Chloro-1-methoxy-2-(3-methoxyphenyl)benzene
• CAS: 565203-84-1
• 化学式: C₁₄H₁₃ClO₂
• 分子量: 248.709
• InChiKey: HDZVNEKJEBCBQQ-UHFFFAOYSA-N

物化性质

• 沸点：
  330.6±27.0 °C(Predicted)
• 密度：
  1.158±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.4
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  18.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-Chloro-1-methoxy-2-(3-methoxyphenyl)benzene 在 二乙基异丙基胺 、 三溴化硼 作用下， 以 二氯甲烷 为溶剂， 生成 Trifluoro-methanesulfonic acid 5-chloro-3'-methoxy-biphenyl-2-yl ester
  参考文献：
  名称：

  Synthesis and biological evaluation of 4-[3-biphenyl-2-yl-1-hydroxy-1-(3-methyl-3H-imidazol-4-yl)-prop-2-ynyl]-1-yl-benzonitrile as novel farnesyltransferase inhibitor

  摘要：

  Farnesyltransferase inhibitors (FTIs) have emerged as a novel class of anti-cancer agents. Analogues of the potent FTI, 4-[3-biphenyl-1-hydroxy-1-(3-methyl-3H-imidazol-4-yl)-prop-2-ynyl]-1-yl-benzonitrile, were synthesized and tested in vitro for their inhibitory activities. The synthesis and detailed biological data of this series of analogues are presented. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(03)00122-7
• 作为产物：
  描述：

  3-甲氧基苯硼酸 、 4-氯-2-碘苯甲醚, 在 四(三苯基膦)钯 作用下， 生成 4-Chloro-1-methoxy-2-(3-methoxyphenyl)benzene
  参考文献：
  名称：

  Synthesis and biological evaluation of 4-[3-biphenyl-2-yl-1-hydroxy-1-(3-methyl-3H-imidazol-4-yl)-prop-2-ynyl]-1-yl-benzonitrile as novel farnesyltransferase inhibitor

  摘要：

  Farnesyltransferase inhibitors (FTIs) have emerged as a novel class of anti-cancer agents. Analogues of the potent FTI, 4-[3-biphenyl-1-hydroxy-1-(3-methyl-3H-imidazol-4-yl)-prop-2-ynyl]-1-yl-benzonitrile, were synthesized and tested in vitro for their inhibitory activities. The synthesis and detailed biological data of this series of analogues are presented. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(03)00122-7

文献信息

• Ortho-metalation of p-chloroanisole: A media study
  作者：D.W Slocum、P Dietzel

  DOI：10.1016/s0040-4039(99)00161-6

  日期：1999.3

  As the chlorophenyl group is a pharmacophore, its stability toward metalation conditions in conjunction with the methoxy substituent was assessed. For p-chloroanisole metalation ortho to the methoxy group was achieved in high yield using increments of THF in cyclohexane; numerous other regimes afforded lower yields and a competing benzyne pathway. (C) 1999 Published by Elsevier Science Ltd. All rights reserved.