ethoxymethyl triethylammonium chloride | 64632-25-3

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: ethoxymethyl triethylammonium chloride
• 英文别名: N-(Ethoxymethyl)-N,N-diethylethanaminium chloride；ethoxymethyl(triethyl)azanium;chloride
• CAS: 64632-25-3
• 化学式: C₉H₂₂NO*Cl
• 分子量: 195.733
• InChiKey: DSQJHJBPTGEROG-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  -1.14
• 重原子数：
  12
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  咪唑 、 ethoxymethyl triethylammonium chloride 以 甲苯 为溶剂， 生成 1-乙氧基甲基-1H-咪唑
  参考文献：
  名称：

  3-Alkoxymethyl-1-(1R,2S,5R)-(−)-menthoxymethylimidazolium salts-based chiral ionic liquids

  摘要：

  A new group of imidazolium salt-based chiral ionic liquids have been prepared and characterized The chiral ionic liquids obtained are stable in air in contact with water and popular organic solvents Their physicochemical properties single-crystal X-ray structures antimicrobial activities and antielectrostatic effects have been determined The chiral ionic liquids synthesized have proven to represent not only potential new solvents in asymmetric synthesis but also effective disinfectants with antielectrostatic activity (C) 2010 Elsevier Ltd All rights reserved

  DOI：

  10.1016/j.tetasy.2010.10.029
• 作为产物：
  描述：

  三乙胺 、 氯甲基乙醚 以 甲苯 为溶剂， 反应 0.25h， 生成 ethoxymethyl triethylammonium chloride
  参考文献：
  名称：

  3-Alkoxymethyl-1-(1R,2S,5R)-(−)-menthoxymethylimidazolium salts-based chiral ionic liquids

  摘要：

  A new group of imidazolium salt-based chiral ionic liquids have been prepared and characterized The chiral ionic liquids obtained are stable in air in contact with water and popular organic solvents Their physicochemical properties single-crystal X-ray structures antimicrobial activities and antielectrostatic effects have been determined The chiral ionic liquids synthesized have proven to represent not only potential new solvents in asymmetric synthesis but also effective disinfectants with antielectrostatic activity (C) 2010 Elsevier Ltd All rights reserved

  DOI：

  10.1016/j.tetasy.2010.10.029

文献信息

• NOVEL SULFONIC ACID DERIVATIVE COMPOUND AND NOVEL NAPHTHALIC ACID DERIVATIVE COMPOUND
  申请人：Murai Toshihiko

  公开号：US20120289697A1

  公开（公告）日：2012-11-15

  Disclosed are a novel sulfonic acid derivative compound and a novel naphthalic acid derivative compound with high solubility in organic solvents, good photosensitivity, and suitability as a photoacid generator and a polymerization initiator. The sulfonic acid derivative compound is represented by the formula (I) (wherein R 01 , R 04 , R 05 , and R 06 represent a hydrogen atom; any one of R 02 and R 03 represents an alkoxy group having a carbon number of 4 to 18 which may be substituted with an alicyclic hydrocarbon group, a heterocyclic group, or a halogen atom and which may have a branch, or the like; and R 07 represents an aliphatic hydrocarbon group having a carbon number of 1 to 18 which may be substituted with a halogen atom and/or an alkylthio group, or the like).

  揭示了一种新颖的磺酸衍生物化合物和一种新颖的萘甲酸衍生物化合物，具有在有机溶剂中高溶解度、良好的光敏性，并适用于光酸发生剂和聚合引发剂。磺酸衍生物化合物由以下式(I)表示（其中R01、R04、R05和R06代表氢原子；R02和R03中的任一表示具有4至18个碳原子的烷氧基，可以被取代为脂环烃基、杂环基或卤素原子，并且可以具有支链等；R07表示具有1至18个碳原子的脂肪烃基，可以被取代为卤素原子和/或烷基硫基等）。
• SULFONIC ACID DERIVATIVE COMPOUND AND NAPHTHALIC ACID DERIVATIVE COMPOUND
  申请人：Adeka Corporation

  公开号：EP2524914B1

  公开（公告）日：2019-07-03
• US8680268B2
  申请人：——

  公开号：US8680268B2

  公开（公告）日：2014-03-25
• 3-Alkoxymethyl-1-(1R,2S,5R)-(−)-menthoxymethylimidazolium salts-based chiral ionic liquids
  作者：Joanna Feder-Kubis、Maciej Kubicki、Juliusz Pernak

  DOI：10.1016/j.tetasy.2010.10.029

  日期：2010.11

  A new group of imidazolium salt-based chiral ionic liquids have been prepared and characterized The chiral ionic liquids obtained are stable in air in contact with water and popular organic solvents Their physicochemical properties single-crystal X-ray structures antimicrobial activities and antielectrostatic effects have been determined The chiral ionic liquids synthesized have proven to represent not only potential new solvents in asymmetric synthesis but also effective disinfectants with antielectrostatic activity (C) 2010 Elsevier Ltd All rights reserved