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erythromycin-9-[O-(2,3-epoxypropyl)]oxime | 93488-70-1

中文名称
——
中文别名
——
英文名称
erythromycin-9-[O-(2,3-epoxypropyl)]oxime
英文别名
——
erythromycin-9-[O-(2,3-epoxypropyl)]oxime化学式
CAS
93488-70-1
化学式
C40H72N2O14
mdl
——
分子量
805.017
InChiKey
VDLZUTHVPMOXLR-HMEKHNNZSA-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):
    1.99
  • 重原子数:
    56.0
  • 可旋转键数:
    10.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.95
  • 拓扑面积:
    210.96
  • 氢给体数:
    5.0
  • 氢受体数:
    16.0

上下游信息

  • 上游原料
    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:
    描述:
    erythromycin-9-[O-(2,3-epoxypropyl)]oxime2-苯乙胺氯仿 为溶剂, 反应 73.0h, 生成 erythromycin-9-[O-(3-(2-phenylethylamino)-2-hydroxy)propyl]oxime
    参考文献:
    名称:
    Synthesis and antimicrobial activity of erythromycin-A oxime analogs
    摘要:
    A series of erythromycin-A oxime ether as well as esters have been synthesized. Ether derivatives were synthesized through the epoxy ether intermediate of erythromycin-9-oxime, followed by opening of the epoxy linkage through various amines, whereas esters have been prepared through DCC mediated protocol. These derivatives have been evaluated for antibacterial activity and found to be as active as erythromycin-A. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2004.05.011
  • 作为产物:
    描述:
    红霉素吡啶盐酸羟胺potassium carbonate 作用下, 以 丙酮 为溶剂, 反应 79.0h, 生成 erythromycin-9-[O-(2,3-epoxypropyl)]oxime
    参考文献:
    名称:
    Synthesis and antimicrobial activity of erythromycin-A oxime analogs
    摘要:
    A series of erythromycin-A oxime ether as well as esters have been synthesized. Ether derivatives were synthesized through the epoxy ether intermediate of erythromycin-9-oxime, followed by opening of the epoxy linkage through various amines, whereas esters have been prepared through DCC mediated protocol. These derivatives have been evaluated for antibacterial activity and found to be as active as erythromycin-A. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2004.05.011
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