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2,3-Dihydroxypropyl hexylcarbamate | 683799-94-2

中文名称
——
中文别名
——
英文名称
2,3-Dihydroxypropyl hexylcarbamate
英文别名
2,3-dihydroxypropyl N-hexylcarbamate
2,3-Dihydroxypropyl hexylcarbamate化学式
CAS
683799-94-2
化学式
C10H21NO4
mdl
——
分子量
219.281
InChiKey
FXEUZKTWHZHRDH-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):
    1
  • 重原子数:
    15
  • 可旋转键数:
    9
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    78.8
  • 氢给体数:
    3
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    羟甲基二氧杂戊环酮正己胺 反应 2.0h, 以9%的产率得到甘油
    参考文献:
    名称:
    碳酸甘油酯在有机和有机介质中的氨解反应
    摘要:
    AbstractAminolysis reaction of glycerol carbonate with primary amine in organic and hydroorganic media leads to the formation of two hydroxyurethane isomers and a partial decomposition of glycerol carbonate into glycerol. Aminolysis with a secondary amine promotes the condensation reaction and limits the formation of glycerol. The ratio of α versus β was determined by zgig 13C NMR. This technique permits computing the yield of α and β products in the medium. The quantity of glycerol was determined by GC analysis. The ratio of the isomers and the amount of glycerol depend on the amine and the solvent. Kinetic investigations reveal that, in hydroorganic medium, the more the alkyl chain of the amine increased, the less glycerol was formed. On the contrary, in organic medium, the alkyl chain of the amine does not play a major role in the formation of glycerol.
    DOI:
    10.1007/s11746-011-1995-5
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文献信息

  • Aminolysis Reaction of Glycerol Carbonate in Organic and Hydroorganic Medium
    作者:Bassam Nohra、Laure Candy、Jean-François Blanco、Yann Raoul、Zephirin Mouloungui
    DOI:10.1007/s11746-011-1995-5
    日期:2012.6
    AbstractAminolysis reaction of glycerol carbonate with primary amine in organic and hydroorganic media leads to the formation of two hydroxyurethane isomers and a partial decomposition of glycerol carbonate into glycerol. Aminolysis with a secondary amine promotes the condensation reaction and limits the formation of glycerol. The ratio of α versus β was determined by zgig 13C NMR. This technique permits computing the yield of α and β products in the medium. The quantity of glycerol was determined by GC analysis. The ratio of the isomers and the amount of glycerol depend on the amine and the solvent. Kinetic investigations reveal that, in hydroorganic medium, the more the alkyl chain of the amine increased, the less glycerol was formed. On the contrary, in organic medium, the alkyl chain of the amine does not play a major role in the formation of glycerol.
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