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1-[4-(4-azido-2-fluoro-phenyl)-piperazin-1-yl]-2-hydroxy-propan-1-one | 864147-47-7

中文名称
——
中文别名
——
英文名称
1-[4-(4-azido-2-fluoro-phenyl)-piperazin-1-yl]-2-hydroxy-propan-1-one
英文别名
1-[4-(4-Azido-2-fluorophenyl)piperazin-1-yl]-2-hydroxypropan-1-one;1-[4-(4-azido-2-fluorophenyl)piperazin-1-yl]-2-hydroxypropan-1-one
1-[4-(4-azido-2-fluoro-phenyl)-piperazin-1-yl]-2-hydroxy-propan-1-one化学式
CAS
864147-47-7
化学式
C13H16FN5O2
mdl
——
分子量
293.301
InChiKey
POMKKNQPRSEASB-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):
    2.1
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    58.1
  • 氢给体数:
    1
  • 氢受体数:
    6

文献信息

  • Oxazolidinone combinatorial libraries, compositions and methods of preparation
    申请人:Gordeev F. Mikhail
    公开号:US20050004174A1
    公开(公告)日:2005-01-06
    Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.
    本发明提供了氧杂环丙烷酮及其合成方法。还提供了包含氧杂环丙烷酮的组合化学文库以及制备这些文库的方法。此外,还提供了制备生物活性氧杂环丙烷酮的方法以及包含氧杂环丙烷酮的药学可接受组合物的方法。文库制备的方法包括将氧杂环丙烷酮附着到固体支持上。在一种实施例中,化合物制备的方法涉及将亚胺酰胺与含有羰基的聚合物支持物反应。
  • [EN] NOVEL TRIAZOLE COMPOUNDS AS ANTIBACTERIAL AGENTS AND THEIR PHARMACEUTICAL COMPOSITIONS CONTAINING THEM<br/>[FR] NOUVEAUX COMPOSES DE TRIAZOLE EN TANT QU'AGENTS ANTIBACTERIENS ET COMPOSITIONS PHARMACEUTIQUES EN CONTENANT
    申请人:REDDYS LAB LTD DR
    公开号:WO2005082892A2
    公开(公告)日:2005-09-09
    The present invention relates to novel triazole compounds of formula (I), where all symbols are as defined in the detailed description; their pharmaceutically acceptable salts their stereosiomers thereof, their prodrugs, their rotamers, their pharmaceutical compositions containing them. The present invention also relates to a process for the preparation of the above said novel compounds.
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