3-(hexadecyloxy)-2-methylphenol | 130442-06-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 3-(hexadecyloxy)-2-methylphenol
• 英文别名: 3-Hexadecoxy-2-methylphenol
• CAS: 130442-06-7
• 化学式: C₂₃H₄₀O₂
• 分子量: 348.569
• InChiKey: XYVSPEATHLBUPE-UHFFFAOYSA-N

物化性质

• 沸点：
  460.7±25.0 °C(Predicted)
• 密度：
  0.927±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  9.7
• 重原子数：
  25
• 可旋转键数：
  16
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.74
• 拓扑面积：
  29.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  3-(hexadecyloxy)-2-methylphenol 在 硫酸 、 sodium hydride 、 sodium iodide 作用下， 以 四氢呋喃 、 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 19.5h， 生成 3-<3-(hexadecyloxy)-2-methylphenoxy>-1,2-propanediol
  参考文献：
  名称：

  Analogs of platelet activating factor. 6. Mono- and bis-aryl phosphate antagonists of platelet activating factor

  摘要：

  A series of aryl phosphoglyceride (3, 19-6 1) and bis-aryl phosphate (67-135) antagonists of platelet activating factor (PAF) were prepared. A group of four bifunctional phosphorus reagents (5a-c and 7) were developed that allowed the preparation of these aryl phosphates in which the position of aromatic substitution can be varied. These compounds were examined for their ability to inhibit PAF-induced platelet aggregation of rabbit platelets. Selected compounds were also evaluated for their ability to displace [H-3]PAF from its receptor on rabbit platelets. These in vitro data were compared to similar data obtained for a number of known PAF antagonists. The compounds were evaluated in vivo, in both the mouse and rabbit, for their ability to prevent death induced by a lethal challenge of PAF. The relationships between the biological activity and the nature, lipophilicity, and position of substituents of the aromatic rings were studied. Compound 105 (CL 184005) has been selected to undergo further development as a potential therapeutic agent for the treatment of septic shock in man.

  DOI：

  10.1021/jm00087a023
• 作为产物：
  描述：

  2,6-二羟基甲苯 、 溴代十六烷 在 sodium iodide 作用下， 以 四氢呋喃 、 正己烷 、 N,N-二甲基甲酰胺 为溶剂， 生成 3-(hexadecyloxy)-2-methylphenol
  参考文献：
  名称：

  Bis-arylphosphate ester antagonists of platelet activating factor

  摘要：

  这项发明是一种新型化合物，化学式为：##STR1##，它们是血小板活化因子的拮抗剂。

  公开号：

  US04983592A1

文献信息

• [EN] A PROCESS FOR THE PREPARATION OF TRIAZINE INTERMEDIATES AND A PROCESS FOR THE PREPARATION OF UV ABSORBERS THEREOF<br/>[FR] PROCÉDÉ DE PRÉPARATION D'INTERMÉDIAIRES DE TRIAZINE ET PROCÉDÉ DE PRÉPARATION D'ABSORBEURS UV ASSOCIÉS
  申请人：BASF SE

  公开号：WO2020144093A1

  公开（公告）日：2020-07-16

  The presently claimed invention relates to a novel, highly efficient and general process for the preparation of the triazine intermediates and their use in the preparation of UV absorbers.

  目前所声称的发明涉及一种新颖、高效和通用的三嗪中间体制备过程及其在制备紫外线吸收剂中的应用。
• Novel bis-arylphosphate ester antagonists of platelet activating factor
  申请人：AMERICAN CYANAMID COMPANY

  公开号：EP0374513A2

  公开（公告）日：1990-06-27

  The invention is novel compounds of the formula: which are antagonists of platelet activating factor.

  本发明是式中的新型化合物： 是血小板活化因子的拮抗剂。
• A PROCESS FOR THE PREPARATION OF TRIAZINE INTERMEDIATES AND A PROCESS FOR THE PREPARATION OF UV ABSORBERS THEREOF
  申请人：BASF SE

  公开号：EP3908633A1

  公开（公告）日：2021-11-17
• US4983592A
  申请人：——

  公开号：US4983592A

  公开（公告）日：1991-01-08
• US5147864A
  申请人：——

  公开号：US5147864A

  公开（公告）日：1992-09-15