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Cα-methyl-D,L-prenylglycinamide | 364784-16-7

中文名称
——
中文别名
——
英文名称
Cα-methyl-D,L-prenylglycinamide
英文别名
2-Amino-2,5-dimethylhex-4-enamide
C<sup>α</sup>-methyl-D,L-prenylglycinamide化学式
CAS
364784-16-7
化学式
C8H16N2O
mdl
——
分子量
156.228
InChiKey
CFKPCPZYXBSXID-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):
    0.4
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    69.1
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    Cα-methyl-D,L-prenylglycinamide 在 Mycobacterium neoaurum ATCC 25795 作用下, 以 溶剂黄146 为溶剂, 生成 Cα-methyl-D-prenylglycinamide 、 Cα-methyl-L-prenylglycinamide 、 Cα-methyl-L-prenylglycine
    参考文献:
    名称:
    Enantiopure Cα-tetrasubstituted α-amino acids. Chemo-enzymatic synthesis and application to turn-forming peptides
    摘要:
    By a chemo-enzymatic approach we carried out a large-scale synthesis of four enantiopure, sterically constrained, C-alpha-tetra-substituted alpha -amino acids, all characterized by a sidechain (CCdelta)-C-gamma double bond. By using one of them (L-Mag), we prepared an N-alpha-protected tetrapeptide benzylamide which was shown to adopt a beta -turn conformation and to efficiently undergo ring-closing olefin metathesis. (C) 2001 Elsevier Science Led. All rights reserved.
    DOI:
    10.1016/s0040-4020(01)00548-8
  • 作为产物:
    描述:
    2,5-Dimethyl-2-{[1-phenyl-meth-(E)-ylidene]-amino}-hex-4-enoic acid amide 在 盐酸 作用下, 生成 Cα-methyl-D,L-prenylglycinamide
    参考文献:
    名称:
    Enantiopure Cα-tetrasubstituted α-amino acids. Chemo-enzymatic synthesis and application to turn-forming peptides
    摘要:
    By a chemo-enzymatic approach we carried out a large-scale synthesis of four enantiopure, sterically constrained, C-alpha-tetra-substituted alpha -amino acids, all characterized by a sidechain (CCdelta)-C-gamma double bond. By using one of them (L-Mag), we prepared an N-alpha-protected tetrapeptide benzylamide which was shown to adopt a beta -turn conformation and to efficiently undergo ring-closing olefin metathesis. (C) 2001 Elsevier Science Led. All rights reserved.
    DOI:
    10.1016/s0040-4020(01)00548-8
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