2-(N-propyl-anilino)-ethanol

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 2-(N-propyl-anilino)-ethanol
• 英文别名: 2-(N-Propyl-anilino)-aethanol；2-(N-n-Propyl-N-phenyl)-aminoethanol；2-(N-propylanilino)ethanol
• 化学式: C₁₁H₁₇NO
• 分子量: 179.262
• InChiKey: URLPJFHFBQWEDB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  13
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  23.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  2-乙基-3-苯基-1,3-恶唑烷 在 1,4-二氧六环 、 lithium aluminium tetrahydride 作用下， 生成 2-(N-propyl-anilino)-ethanol
  参考文献：
  名称：

  The Cleavage of Oxazolidines by Lithium Aluminum Hydride

  摘要：

  DOI：

  10.1021/ja01156a051

文献信息

• PROCESSES FOR THE PREPARATION OF PESTICIDAL COMPOUNDS
  申请人：Dow AgroSciences LLC

  公开号：US20180186734A1

  公开（公告）日：2018-07-05

  The disclosure relates to efficient and economical synthetic chemical processes for the preparation of pesticidal thioethers. Further, the disclosure relates to certain novel compounds useful in the preparation of pesticidal thioethers.

  该披露涉及用于制备杀虫硫醚的高效经济合成化学过程。此外，该披露涉及用于制备杀虫硫醚的特定新化合物。
• An environmentally safe method of preparing a certain dialkylamine
  申请人：MAKHTESHIM CHEMICAL WORKS LIMITED

  公开号：EP0403952A2

  公开（公告）日：1990-12-27

  N-n-propyl-N-2-(2,4,6-trichlorophenoxy) ethyl amine is prepared by reacting 2-phenoxy ethanol with thionyl chloride in the presence of a catalytic amount of tetra-alkyl ammonium halide optionally in the presence of a solvent to form 2-phenoxy ethyl chloride; reacting the 2-phenoxy ethyl chloride with n-propylamine at a temp-erature of from 50°C to 150°C optionally in the presence of a solvent to form N-n-propyl-N-2-phenoxy-ethyl amine; selectively chlorinating N-n-propyl-N-2-phenoxyethyl amine with chlorine in the presence of a solvent; and recovering the N-n-propyl-N-2-(2,4,6-trichlorophenoxy) ethyl amine formed.

  N-正丙基-N-2-(2,4,6-三氯苯氧基)乙基胺的制备方法是：在催化量的四烷基卤化铵存在下，任选在溶剂存在下，使 2-苯氧基乙醇与亚硫酰氯反应生成 2-苯氧基乙基氯；将 2-苯氧基乙基氯与正丙胺在 50°C 至 150°C 的温度下反应，生成 N-正丙基-N-2-苯氧基乙基胺；在有溶剂存在的情况下，选择性地用氯将 N-正丙基-N-2-苯氧基乙基胺氯化；回收生成的 N-正丙基-N-2-（2,4,6-三氯苯氧基）乙基胺。
• Baxter et al., Journal of the Chemical Society, 1955, p. 669,674
  作者：Baxter et al.

  DOI：——

  日期：——
• FLUORESCENCE QUENCHING AZO DYES, THEIR METHODS OF PREPARATION AND USE
  申请人：Laikhter Andrei

  公开号：US20090053821A1

  公开（公告）日：2009-02-26

  Disclosed is a group of azo quencher compositions useful as fluorescence quenchers having the general structure of formula 1, methods of making or using the compositions, and kits comprising the composition.
• Cure accelerators for anaerobic curable compositions
  申请人：Messana Andrew

  公开号：US20090278084A1

  公开（公告）日：2009-11-12

  The present invention provides compounds represented by structural Formula (III): wherein X, R 1 , R 2 , and R 4 are as described herein, reaction products of compounds of Formula (III) and isocyanates, use of such compounds and reaction products as anaerobic cure accelerators, methods of making the same, and compositions including such compounds.