4-Amino-2-sec-butyl-phenol | 13781-16-3

• 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-Amino-2-sec-butyl-phenol
• 英文别名: 4-Amino-2-(butan-2-yl)phenol；4-amino-2-butan-2-ylphenol
• CAS: 13781-16-3
• 化学式: C₁₀H₁₅NO
• 分子量: 165.235
• InChiKey: JUSBZKRCCQLICT-UHFFFAOYSA-N

物化性质

• 沸点：
  303.4±30.0 °C(Predicted)
• 密度：
  1.054±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  46.2
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-Amino-2-sec-butyl-phenol 以 四氢呋喃 、 甲醇 、 乙醇 为溶剂， 反应 48.5h， 生成 N-[3-butan-2-yl-5-(diethylaminomethyl)-4-hydroxyphenyl]acetamide
  参考文献：
  名称：

  Antimalarial drugs. 61. Synthesis and antimalarial effects of 4-[(7-chloro-4-quinolinyl)amino]-2-[(diethylamino)methyl]-6-alkylphenols and their N.omega.-oxides

  摘要：

  A series of 4-[(7-chloro-4-quinolinyl)amino]-2-[(diethylamino)methyl]-6-alkylphenols and their N omega-oxides were synthesized by the condensation of 4,7-dichloroquinoline and 4,7-dichloroquinoline N omega-oxide with appropriately substituted 4-amino-2-[(diethylamino)methyl]-6-alkylphenol dihydrochlorides. The latter precursors were prepared in a six-step synthesis starting from available 2-alkylphenols. Several of the title compounds display potent antimalarial activity in mice.

  DOI：

  10.1021/jm00388a027
• 作为产物：
  描述：

  2-仲丁基苯酚 在 镍 盐酸 、 氢气 、 sodium nitrite 作用下， 以 甲醇 、 乙醇 为溶剂， 反应 10.5h， 生成 4-Amino-2-sec-butyl-phenol
  参考文献：
  名称：

  Antimalarial drugs. 61. Synthesis and antimalarial effects of 4-[(7-chloro-4-quinolinyl)amino]-2-[(diethylamino)methyl]-6-alkylphenols and their N.omega.-oxides

  摘要：

  A series of 4-[(7-chloro-4-quinolinyl)amino]-2-[(diethylamino)methyl]-6-alkylphenols and their N omega-oxides were synthesized by the condensation of 4,7-dichloroquinoline and 4,7-dichloroquinoline N omega-oxide with appropriately substituted 4-amino-2-[(diethylamino)methyl]-6-alkylphenol dihydrochlorides. The latter precursors were prepared in a six-step synthesis starting from available 2-alkylphenols. Several of the title compounds display potent antimalarial activity in mice.

  DOI：

  10.1021/jm00388a027

文献信息

• Azaoxa heterocyclic compound and method of preparing the same
  申请人：——

  公开号：US20040068084A1

  公开（公告）日：2004-04-08

  Disclosed is an azaoxa heterocyclic compound represented by the following formula (I): 1 (wherein, each symbol is defined the same as in the specification) and a method for preparing the same. This compound of the present invention is prepared by the reaction of a phenolic compound, an aromatic diamine compound and an aldehyde compound. The azaoxa heterocyclic compound of the present invention can be used as a hardening resin or a hardener for an epoxy resin, polyether and a resin containing active hydrogen atoms, wherein the composition formed by the azaoxa heterocyclic compound and the epoxy resin is useful in the application of laminates, adhesive, semiconductor packaging materials and phenolic resin forming materials.

  本发明公开了由下式(I)代表的氮杂环化合物： 1 (其中，各符号的定义与说明书中相同）及其制备方法。本发明的这种化合物是由酚类化合物、芳香二胺化合物和醛化合物反应制备的。本发明的氮杂环化合物可用作硬化树脂或环氧树脂、聚醚和含有活泼氢原子的树脂的硬化剂，其中氮杂环化合物和环氧树脂形成的组合物可用于层压板、粘合剂、半导体包装材料和酚醛树脂成型材料。
• US4059567A
  申请人：——

  公开号：US4059567A

  公开（公告）日：1977-11-22
• US4094861A
  申请人：——

  公开号：US4094861A

  公开（公告）日：1978-06-13
• US7202359B2
  申请人：——

  公开号：US7202359B2

  公开（公告）日：2007-04-10
• Antimalarial drugs. 61. Synthesis and antimalarial effects of 4-[(7-chloro-4-quinolinyl)amino]-2-[(diethylamino)methyl]-6-alkylphenols and their N.omega.-oxides
  作者：Stephen J. Kesten、Judith Johnson、Leslie M. Werbel

  DOI：10.1021/jm00388a027

  日期：1987.5

  A series of 4-[(7-chloro-4-quinolinyl)amino]-2-[(diethylamino)methyl]-6-alkylphenols and their N omega-oxides were synthesized by the condensation of 4,7-dichloroquinoline and 4,7-dichloroquinoline N omega-oxide with appropriately substituted 4-amino-2-[(diethylamino)methyl]-6-alkylphenol dihydrochlorides. The latter precursors were prepared in a six-step synthesis starting from available 2-alkylphenols. Several of the title compounds display potent antimalarial activity in mice.