1,2,2,3-四甲基咪唑烷 | 33709-65-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑烷类
• 中文名称: 1,2,2,3-四甲基咪唑烷
• 英文名称: 1,2,2,3-Tetramethyl-imidazolidin
• 英文别名: Imidazolidine, 1,2,2,3-tetramethyl-；1,2,2,3-tetramethylimidazolidine
• CAS: 33709-65-8
• 化学式: C₇H₁₆N₂
• 分子量: 128.217
• InChiKey: NAADVJQGVMQUNR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.8
• 重原子数：
  9
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  6.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  borane tetrahydrofuran 、 1,2,2,3-四甲基咪唑烷 以 四氢呋喃 为溶剂， 生成
  参考文献：
  名称：

  11B Nuclear magnetic resonance study of the reactivity of borane tetrahydrofuran with representative dithianes, diazolidines, thiazolidines, benzothiazolines and benzothiazoles

  摘要：

  DOI：

  10.1016/0584-8539(87)80197-6
• 作为产物：
  描述：

  N,N-dimethyl-1-[2-(1,2,3-trimethyl-1,3,2-diazasilolidin-2-yl)phenyl]methanamine 、 丙酮 以 氘代氯仿 为溶剂， 反应 24.0h， 生成 1,2,2,3-四甲基咪唑烷
  参考文献：
  名称：

  Aminosilylation of heterocumulenes and the intramolecular decomposition of their silyl-functionalized adducts

  摘要：

  Heteroorganic amidosilanes are readily obtained by interaction of CO2, CS2 and other heterocumulenes with pentacoordinated diaminosilanes. A comparison is made with the corresponding reactions of tetracoordinated species. Decomposition of these bifunctional organosilanes gives 2-substituted ureido derivatives and base-stabilized low coordinated silicon species, seemingly by a unimolecular thermal beta-elimination.

  DOI：

  10.1016/0022-328x(91)86160-r

文献信息

• Polycyclic agents for the treatment of respiratory syncytial virus infections
  申请人：Bond Silas

  公开号：US20070287700A1

  公开（公告）日：2007-12-13

  Compounds of formula (I), and their use as in the treatment of infections involving viruses of the Pneumovirinae sub-family (RSV) are disclosed. In the formula ring (A) may be phenyl, pyridyl etc., (B-C) may be CH 2 —CH 2 etc., (R 1 ) may be phenyl and substituted forms thereof, (R 2 ) may be assorted substituents.

  本发明公开了化学式(I)的化合物及其在治疗涉及Pneumovirinae亚科（RSV）病毒感染中的应用。在该式中，环（A）可以是苯基、吡啶基等，（B-C）可以是CH2-CH2等，（R1）可以是苯基及其取代形式，（R2）可以是不同的取代基。
• Polycyclic Agents for the Treatment of Respiratory Syncytial Virus Infections
  申请人：Biota Scientific Management Pty Ltd.

  公开号：US20140051689A1

  公开（公告）日：2014-02-20

  Compounds of formula (I), and their use as in the treatment of infections involving viruses of the Pneumovirinae sub-family (RSV) are disclosed. In the formula ring (A) may be phenyl, pyridyl etc., (B-C) may be CH 2 —CH 2 etc., (R 1 ) may be phenyl and substituted forms thereof, (R 2 ) may be assorted substituents.

  本发明涉及化合物(I)的公式及其在治疗涉及Pneumovirinae亚科病毒（RSV）感染方面的用途。在该公式中，环(A)可以是苯基、吡啶基等，(B-C)可以是CH2-CH2等，(R1)可以是苯基及其取代形式，(R2)可以是各种取代基。
• ZIRCONIUM, HAFNIUM, TITANIUM, AND SILICON PRECURSORS FOR ALD/CVD
  申请人：Xu Chongying

  公开号：US20100112211A1

  公开（公告）日：2010-05-06

  Zirconium, hafnium, titanium and silicon precursors useful for atomic layer deposition (ALD) and chemical vapor deposition (CVD) of corresponding zirconium-containing, hafnium-containing, titanium-containing and silicon-containing films, respectively. The disclosed precursors achieve highly conformal deposited films characterized by minimal carbon incorporation.
• 11B Nuclear magnetic resonance study of the reactivity of borane tetrahydrofuran with representative dithianes, diazolidines, thiazolidines, benzothiazolines and benzothiazoles
  作者：Rosalinda Contreras、Hilda R. Morales、Ma. de Lourdes Mendoza、Cesar Dominguez

  DOI：10.1016/0584-8539(87)80197-6

  日期：1987.1
• Aminosilylation of heterocumulenes and the intramolecular decomposition of their silyl-functionalized adducts
  作者：R.J.P. Corriu、Gérard F. Lanneau、V.D. Mehta

  DOI：10.1016/0022-328x(91)86160-r

  日期：1991.11

  Heteroorganic amidosilanes are readily obtained by interaction of CO2, CS2 and other heterocumulenes with pentacoordinated diaminosilanes. A comparison is made with the corresponding reactions of tetracoordinated species. Decomposition of these bifunctional organosilanes gives 2-substituted ureido derivatives and base-stabilized low coordinated silicon species, seemingly by a unimolecular thermal beta-elimination.