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2,3-O-isopropylidene-D-glyceroamidoxime | 1262023-53-9

中文名称
——
中文别名
——
英文名称
2,3-O-isopropylidene-D-glyceroamidoxime
英文别名
(4S)-N'-hydroxy-2,2-dimethyl-1,3-dioxolane-4-carboximidamide
2,3-O-isopropylidene-D-glyceroamidoxime化学式
CAS
1262023-53-9
化学式
C6H12N2O3
mdl
——
分子量
160.173
InChiKey
ZDRPPUWHXRKSNP-SCSAIBSYSA-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

物化性质

  • 沸点:
    242.9±50.0 °C(Predicted)
  • 密度:
    1.38±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.3
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    77.1
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    2,3-O-isopropylidene-D-glyceroamidoxime苯甲酸N,N'-二环己基碳二亚胺 作用下, 以 二氯甲烷 为溶剂, 反应 7.0h, 以78%的产率得到5-phenyl-3-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-1,2,4-oxadiazole
    参考文献:
    名称:
    Synthesis and antiacetylcholinesterase activity of new D-glyceraldehyde heterocyclic derivatives
    摘要:
    We report herein the convenient procedures for the syntheses of different heterocyclic compounds from 2,3-O-isopropylidene-D-glyceraldehyde using intramolecular cyclization, 1,3-dipolar cycloaddition or bimolecular coupling reactions. The products were characterized by H-1 and C-13 NMR spectroscopy and elemental analysis. The new heterocycles and their derivatives were evaluated as inhibitors of acetylcholinesterase enzyme.
    DOI:
    10.1590/s0103-50532010000100008
  • 作为产物:
    描述:
    2,3-O-isopropylidene-D-glyceronitrile盐酸羟胺sodium carbonate 作用下, 以 甲醇 为溶剂, 以57%的产率得到2,3-O-isopropylidene-D-glyceroamidoxime
    参考文献:
    名称:
    Synthesis and antiacetylcholinesterase activity of new D-glyceraldehyde heterocyclic derivatives
    摘要:
    We report herein the convenient procedures for the syntheses of different heterocyclic compounds from 2,3-O-isopropylidene-D-glyceraldehyde using intramolecular cyclization, 1,3-dipolar cycloaddition or bimolecular coupling reactions. The products were characterized by H-1 and C-13 NMR spectroscopy and elemental analysis. The new heterocycles and their derivatives were evaluated as inhibitors of acetylcholinesterase enzyme.
    DOI:
    10.1590/s0103-50532010000100008
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