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N-cyclopropyl-1-[4-(trifluoromethoxy)benzyl]-1H-tetrazol-5-amine | 1353642-05-3

中文名称
——
中文别名
——
英文名称
N-cyclopropyl-1-[4-(trifluoromethoxy)benzyl]-1H-tetrazol-5-amine
英文别名
N-cyclopropyl-1-[[4-(trifluoromethoxy)phenyl]methyl]tetrazol-5-amine
N-cyclopropyl-1-[4-(trifluoromethoxy)benzyl]-1H-tetrazol-5-amine化学式
CAS
1353642-05-3
化学式
C12H12F3N5O
mdl
——
分子量
299.255
InChiKey
VYVYCWSUZZQTDK-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):
    3.2
  • 重原子数:
    21
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    64.9
  • 氢给体数:
    1
  • 氢受体数:
    8

反应信息

  • 作为产物:
    参考文献:
    名称:
    1-Alkyl-5-((di)alkylamino) Tetrazoles: Building Blocks for Peptide Surrogates
    摘要:
    An approach to the synthesis of 1-alkyl-5-((di)allcylamino)tetrazoles by nucleophilic substitution in 1-alkyl-5-sulfonyl-tetrazoles with anions generated from the primary secondary amines was developed. Tolerance of the method to the presence of some functional groups (i.e., protected amine) in both components of the reaction was demonstrated. Obtained tetrazoles are promising building blocks for the design of peptide surrogates, in particular, for replacement approaches of alkyl urea derivatives.
    DOI:
    10.1021/jo2022235
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文献信息

  • 1-Alkyl-5-((di)alkylamino) Tetrazoles: Building Blocks for Peptide Surrogates
    作者:Andriy V. Tymtsunik、Vitaliy A. Bilenko、Serhiy O. Kokhan、Oleksandr O. Grygorenko、Dmitriy M. Volochnyuk、Igor V. Komarov
    DOI:10.1021/jo2022235
    日期:2012.1.20
    An approach to the synthesis of 1-alkyl-5-((di)allcylamino)tetrazoles by nucleophilic substitution in 1-alkyl-5-sulfonyl-tetrazoles with anions generated from the primary secondary amines was developed. Tolerance of the method to the presence of some functional groups (i.e., protected amine) in both components of the reaction was demonstrated. Obtained tetrazoles are promising building blocks for the design of peptide surrogates, in particular, for replacement approaches of alkyl urea derivatives.
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