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3-((4-((2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl)coumarin | 1258307-24-2

中文名称
——
中文别名
——
英文名称
3-((4-((2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl)coumarin
英文别名
[(2R,3S,4S,5R,6R)-3,4,5-triacetyloxy-6-[[1-[(2-oxochromen-3-yl)methyl]triazol-4-yl]methoxy]oxan-2-yl]methyl acetate
3-((4-((2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl)coumarin化学式
CAS
1258307-24-2
化学式
C27H29N3O12
mdl
——
分子量
587.54
InChiKey
VTWQGDHWXIQYOG-SRFJDDQZSA-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:
    699.3±65.0 °C(Predicted)
  • 密度:
    1.46±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    42
  • 可旋转键数:
    14
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    181
  • 氢给体数:
    0
  • 氢受体数:
    14

反应信息

  • 作为产物:
    描述:
    3-(azidomethyl)-2H-chromen-2-one2-propynyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosidecopper(ll) sulfate pentahydratesodium ascorbate 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以65%的产率得到3-((4-((2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl)coumarin
    参考文献:
    名称:
    Expedient synthesis of coumarin-coupled triazoles via ‘click chemistry’ leading to the formation of coumarin–triazole–sugar hybrids
    摘要:
    Coumarin-based triazoles were synthesized from 3-azidomethylcoumarin and a terminal acetylenic compound. Uncatalysed thermal conditions result in a mixture of both 1,4- and 1,5-regioisomers or the thermodynamically more stable 1,4-regioisomer, whereas the Cu(I)-catalysed reaction affords only the favourable 1,4-regioisomer. B3LYP/6-31G(d) level of theory has been used to calculate geometry and frequency features of the reactants, transition states (TSs) and products. Computational studies further reveal that 1,4-regioisomeric products are more favourable and also thermodynamically more stable compared to the 1,5-regioisomers. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2010.07.037
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