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| 1448441-35-7

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1448441-35-7
化学式
C21H40O8Si
mdl
——
分子量
448.629
InChiKey
PYTWBJYITJFZIO-YPLQCARHSA-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:
    485.6±45.0 °C(predicted)
  • 密度:
    1.12±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.78
  • 重原子数:
    30.0
  • 可旋转键数:
    6.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    84.84
  • 氢给体数:
    1.0
  • 氢受体数:
    8.0

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    A stereoselective method for the construction of the C8′–O–C6″ ether of nigricanoside-A: synthesis of simple models for the C20 lipid chain/galactosyl glycerol segment
    摘要:
    A method for the stereoselective construction of the C8'-O-C6" ether of nigricanoside-A, an antimitotic natural product from the green alga Avrainvillea nigricans, has been developed based on chirality-transferring Ireland-Claisen rearrangement. The method was successfully applied to the synthesis of simple models for the C20 lipid chain/galactosyl glycerol segment of the natural product. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.06.085
  • 作为产物:
    描述:
    四丁基氟化铵溶剂黄146 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以80%的产率得到
    参考文献:
    名称:
    A stereoselective method for the construction of the C8′–O–C6″ ether of nigricanoside-A: synthesis of simple models for the C20 lipid chain/galactosyl glycerol segment
    摘要:
    A method for the stereoselective construction of the C8'-O-C6" ether of nigricanoside-A, an antimitotic natural product from the green alga Avrainvillea nigricans, has been developed based on chirality-transferring Ireland-Claisen rearrangement. The method was successfully applied to the synthesis of simple models for the C20 lipid chain/galactosyl glycerol segment of the natural product. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.06.085
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