4-(Bromomethyl)-[1,1-biphenyl]-2-carboxylicacid | 1187238-04-5

• 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-(Bromomethyl)-[1,1-biphenyl]-2-carboxylicacid
• 英文别名: 5-(bromomethyl)-2-phenylbenzoic acid
• CAS: 1187238-04-5
• 化学式: C₁₄H₁₁BrO₂
• 分子量: 291.144
• InChiKey: AEZZBRBDJNUXBJ-UHFFFAOYSA-N

物化性质

• 沸点：
  410.3±40.0 °C(Predicted)
• 密度：
  1.479±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-(Bromomethyl)-[1,1-biphenyl]-2-carboxylicacid 、 (7S)-7-氨基-1,2,3-三甲氧基-10-甲硫基-6,7-二氢-5H-苯并[g]庚搭烯-9-酮 在 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 (S)-4-(bromomethyl)-N-(1,2,3-trimethoxy-10-(methylthio)-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-7-yl)-[1,1'-biphenyl]-2-carboxamide
  参考文献：
  名称：

  Design, synthesis and identification of novel colchicine-derived immunosuppressant

  摘要：

  Synthesis and biological evaluation of various colchicine analogues through the mixed-lymphocyte reaction (MLR), lymphoproliferation, and inhibitory effects on the inflammatory genes are described. In addition, a new series of immunosuppressive agents developed on the structural basis of colchicine, as well as their structure-activity relationships is reported. The most potent analogue 20a exhibited an excellent immunosuppressive activity on in vivo skin-allograft model, which is comparable to that of cyclosporin A. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.05.054
• 作为产物：
  描述：

  methyl 4-(bromomethyl)[1,1'-biphenyl]-2-carboxylate 在 水 作用下， 以 甲醇 为溶剂， 生成 4-(Bromomethyl)-[1,1-biphenyl]-2-carboxylicacid 、 C₁₄H₁₂O₃
  参考文献：
  名称：

  Design, synthesis and identification of novel colchicine-derived immunosuppressant

  摘要：

  Synthesis and biological evaluation of various colchicine analogues through the mixed-lymphocyte reaction (MLR), lymphoproliferation, and inhibitory effects on the inflammatory genes are described. In addition, a new series of immunosuppressive agents developed on the structural basis of colchicine, as well as their structure-activity relationships is reported. The most potent analogue 20a exhibited an excellent immunosuppressive activity on in vivo skin-allograft model, which is comparable to that of cyclosporin A. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.05.054

文献信息

• Substituted pyrrole, pyrazole and triazole angiotensin II antagonists
  申请人：E.I. DU PONT DE NEMOURS AND COMPANY

  公开号：EP0323841A2

  公开（公告）日：1989-07-12

  Substituted pyrroles, pyrazoles and triazoles such as and their pharmaceutically suitable salts are useful as antihypertensive agents and for treatment of congestive heart failure.

  取代的吡咯、吡唑和三唑，如 及其药用盐类可用作降压药和治疗充血性心力衰竭。
• IMIDAZOLE ETHERS HAVING A II ANTAGONIST ACTIVITY
  申请人：INSTITUTO LUSO FARMACO D'ITALIA S.p.a.

  公开号：EP0652869A1

  公开（公告）日：1995-05-17
• BENZO-FUSED MACROCYCLES PROMOTE RELEASE OF GROWTH HORMONE
  申请人：Merck & Co., Inc.

  公开号：EP0726901A1

  公开（公告）日：1996-08-21
• EP0726901A4
  申请人：——

  公开号：EP0726901A4

  公开（公告）日：1997-01-22
• US5470975A
  申请人：——

  公开号：US5470975A

  公开（公告）日：1995-11-28