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3-azido-1-(4-(1-cyclohexanol)-1H-1,2,3-triazol-1-yl)propan-2-ol | 1612222-50-0

中文名称
——
中文别名
——
英文名称
3-azido-1-(4-(1-cyclohexanol)-1H-1,2,3-triazol-1-yl)propan-2-ol
英文别名
——
3-azido-1-(4-(1-cyclohexanol)-1H-1,2,3-triazol-1-yl)propan-2-ol化学式
CAS
1612222-50-0
化学式
C11H18N6O2
mdl
——
分子量
266.303
InChiKey
ROMPYVGRCMGTMB-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):
    1.1
  • 重原子数:
    19.0
  • 可旋转键数:
    5.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    119.93
  • 氢给体数:
    2.0
  • 氢受体数:
    6.0

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Click Chemistry Inspired Synthesis of Morpholine-Fused Triazoles
    摘要:
    The synthesis of triazolyl azido alcohols from terminal alkyne via oxirane ring-opening of epichlorohydrin, followed by click reaction with alkynes, and subsequent azidation of chlorohydroxy triazoles was achieved under a one-pot methodology. The developed triazolyl azido alcohols were further utilized for the synthesis of a diverse range of morpholine-fused triazoles of chemotherapeutic value. The structure of all developed compounds has been elucidated using IR. NMR, MS, and elemental analysis, where four of them have been characterized by single-crystal X-ray analysis.
    DOI:
    10.1021/jo500890w
  • 作为产物:
    描述:
    炔环己醇环氧氯丙烷 在 sodium azide 、 Cu*O4S(2-)*5H2O 、 sodium ascorbate 作用下, 以 为溶剂, 以45%的产率得到3-azido-1-(4-(1-cyclohexanol)-1H-1,2,3-triazol-1-yl)propan-2-ol
    参考文献:
    名称:
    Click Chemistry Inspired Synthesis of Morpholine-Fused Triazoles
    摘要:
    The synthesis of triazolyl azido alcohols from terminal alkyne via oxirane ring-opening of epichlorohydrin, followed by click reaction with alkynes, and subsequent azidation of chlorohydroxy triazoles was achieved under a one-pot methodology. The developed triazolyl azido alcohols were further utilized for the synthesis of a diverse range of morpholine-fused triazoles of chemotherapeutic value. The structure of all developed compounds has been elucidated using IR. NMR, MS, and elemental analysis, where four of them have been characterized by single-crystal X-ray analysis.
    DOI:
    10.1021/jo500890w
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