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| 1001847-06-8

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1001847-06-8
化学式
C63H77F2NO16Si
mdl
——
分子量
1170.38
InChiKey
CDYBJASZCFYNMB-DEFURMSNSA-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):
    10.21
  • 重原子数:
    83.0
  • 可旋转键数:
    30.0
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    175.39
  • 氢给体数:
    1.0
  • 氢受体数:
    16.0

反应信息

  • 作为反应物:
    描述:
    吡啶四氧化锇 作用下, 反应 3.5h, 以90%的产率得到
    参考文献:
    名称:
    Stereocontrolled and Convergent Entry to CF2-Sialosides:  Synthesis of CF2-Linked Ganglioside GM4
    摘要:
    Sialidase-resistant ganglioside analogues having biological activities similar to those of natural gangliosides are expected to be important probes for clarifying the biological functions of gangliosides. Focusing on difluoromethylene-linked (CF2-linked) alpha(2,3) sialylgalactose as a core structure of sialidase-resistant ganglioside mimics, we have developed novel, stereocontrolled, and efficient methodologies to synthesize CF2-sialosides based on Ireland-Claisen rearrangement. CF2-linked alpha(2,3)sialylgalactose and CF2-linked GM4 were synthesized.
    DOI:
    10.1021/ja075738w
  • 作为产物:
    描述:
    氢氧化钾4-二甲氨基吡啶盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 16.0h, 以77%的产率得到
    参考文献:
    名称:
    Stereocontrolled and Convergent Entry to CF2-Sialosides:  Synthesis of CF2-Linked Ganglioside GM4
    摘要:
    Sialidase-resistant ganglioside analogues having biological activities similar to those of natural gangliosides are expected to be important probes for clarifying the biological functions of gangliosides. Focusing on difluoromethylene-linked (CF2-linked) alpha(2,3) sialylgalactose as a core structure of sialidase-resistant ganglioside mimics, we have developed novel, stereocontrolled, and efficient methodologies to synthesize CF2-sialosides based on Ireland-Claisen rearrangement. CF2-linked alpha(2,3)sialylgalactose and CF2-linked GM4 were synthesized.
    DOI:
    10.1021/ja075738w
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