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(2S)-4-methyl-2-[5-[(4R)-3-[(2-methylpropan-2-yl)oxycarbonyl]-1,3-oxazolidin-4-yl]pyrazol-1-yl]pentanoic acid | 258830-42-1

中文名称
——
中文别名
——
英文名称
(2S)-4-methyl-2-[5-[(4R)-3-[(2-methylpropan-2-yl)oxycarbonyl]-1,3-oxazolidin-4-yl]pyrazol-1-yl]pentanoic acid
英文别名
——
(2S)-4-methyl-2-[5-[(4R)-3-[(2-methylpropan-2-yl)oxycarbonyl]-1,3-oxazolidin-4-yl]pyrazol-1-yl]pentanoic acid化学式
CAS
258830-42-1
化学式
C17H27N3O5
mdl
——
分子量
353.418
InChiKey
BIBWIZAQDAVSHZ-KBPBESRZSA-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:
    25
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    93.9
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    参考文献:
    名称:
    New pyrazole containing bicarboxylic α-amino acids: mimics of the cis amide bond
    摘要:
    A series of novel optically active oc-amino acids, containing a pyrazole ring, which can be regarded as building blocks for peptidomimetics, have been prepared starting from readily available oc-amino acids. The synthetic strategy employed allows the regio- and stereoselective preparation of 1,3- or 1,5-substituted pyrazolyl rings. The pyrazole containing peptidomimetics can be considered as analogues of peptides with a cis amide bond. (C) 1999 Elsevier Science Ltd, All rights reserved.
    DOI:
    10.1016/s0040-4039(99)01847-x
  • 作为产物:
    参考文献:
    名称:
    New pyrazole containing bicarboxylic α-amino acids: mimics of the cis amide bond
    摘要:
    A series of novel optically active oc-amino acids, containing a pyrazole ring, which can be regarded as building blocks for peptidomimetics, have been prepared starting from readily available oc-amino acids. The synthetic strategy employed allows the regio- and stereoselective preparation of 1,3- or 1,5-substituted pyrazolyl rings. The pyrazole containing peptidomimetics can be considered as analogues of peptides with a cis amide bond. (C) 1999 Elsevier Science Ltd, All rights reserved.
    DOI:
    10.1016/s0040-4039(99)01847-x
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