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1-isopropoxy-3,3,7,7-tetramethyl-2,8,9-trioxa-5-aza-1-germatricyclo[3.3.3.O(1,5)]undecane | 1326705-73-0

中文名称
——
中文别名
——
英文名称
1-isopropoxy-3,3,7,7-tetramethyl-2,8,9-trioxa-5-aza-1-germatricyclo[3.3.3.O(1,5)]undecane
英文别名
Ge[(OCH2CH2)N(CH2CMe2O)2](OCH(CH3)2);Ge[imino-2,2,2',2'-tetramethyl-2,2',2''-triethanol-3H](OCH(CH3)2)
1-isopropoxy-3,3,7,7-tetramethyl-2,8,9-trioxa-5-aza-1-germatricyclo[3.3.3.O(1,5)]undecane化学式
CAS
1326705-73-0
化学式
C13H27GeNO4
mdl
——
分子量
333.952
InChiKey
GKIVGXIQIGJFMS-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为产物:
    描述:
    bis(2-methyl-2-hydroxypropyl)(2-hydroxyethyl)aminegermanium tetra-isopropoxide甲苯 为溶剂, 以81%的产率得到1-isopropoxy-3,3,7,7-tetramethyl-2,8,9-trioxa-5-aza-1-germatricyclo[3.3.3.O(1,5)]undecane
    参考文献:
    名称:
    Synthesis and X-ray diffraction analysis/crystal structure of new germatranes containing methyl substituents in three five-membered chelating rings
    摘要:
    Three monomeric germatranes, 1-isopropoxy-3,3,7,7,10,10-hexamethyl-2,8,9-trioxa-5-aza-1-germatricyclo[3.3.3.0(1.5)]undecane (1), 1-isopropoxy-3,3,7,7-tetramethyl-2,8,9-trioxa-5-aza-1-germatricyclo[3.33.0(1.5)]undecane (2), and 1-isopropoxy-3,3-dimethyl-2,8,9-trioxa-5-aza-1-germatricyclo[3.3.3.0(1.5)]undecane (3) have been synthesized by the reaction of Ge(O-i-Pr)(4) in refluxing toluene with corresponding triethanolamines, (HOCH2CH2)(n)N(CH2CMe2OH)(3-n) (n = 0, L1H(3); n = 1, L2H(3); n = 2, L3H(3)), where the number of CMe2 groups adjacent to a OH functionality varied from 3 (L1H(3)) to 2 (L2H(3)), and to 1 (L3H(3)). These germatranes 1-3 have been characterized by solution H-1 and C-13{H-1) NMR and the solid state structure of 2 has been determined by single crystal X-ray diffraction. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2011.06.013
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