摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-(2-Chloroethyl)imidazol-4-amine | 1027031-86-2

中文名称
——
中文别名
——
英文名称
3-(2-Chloroethyl)imidazol-4-amine
英文别名
——
3-(2-Chloroethyl)imidazol-4-amine化学式
CAS
1027031-86-2
化学式
C5H8ClN3
mdl
——
分子量
145.592
InChiKey
BQUNGBBGHCZXKF-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):
    0.2
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    43.8
  • 氢给体数:
    1
  • 氢受体数:
    2

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:
    参考文献:
    名称:
    Routes toN-vinyl-nitroimidazoles andN-vinyl-deazapurines
    摘要:
    AbstractThe preparations of 4‐ and 5‐nitro‐1‐vinylimidazole (2 and 7) are described. Selective reduction of the nitro group using Fe/dil.HCl is achieved for the 4‐nitro derivative but this is not effective when ethoxymethylenemalononitrile is used to trap the amine. For 5‐nitroimidazole studies the N‐vinyl substituent is kept masked as a 2‐chloroethyl group, which remains unchanged during catalytic reduction of the nitro function (Pd/C), and is revealed by HCl elimination at a later stage. In this way, the 1‐deazapurine 13 and the tricyclic derivative 14 have been prepared.
    DOI:
    10.1002/jhet.5570410508
  • 作为产物:
    描述:
    1-(2-氯乙基)-5-硝基-1H-咪唑 在 palladium on activated charcoal 氢气 作用下, 以 1,4-二氧六环 为溶剂, 生成 3-(2-Chloroethyl)imidazol-4-amine
    参考文献:
    名称:
    Routes toN-vinyl-nitroimidazoles andN-vinyl-deazapurines
    摘要:
    AbstractThe preparations of 4‐ and 5‐nitro‐1‐vinylimidazole (2 and 7) are described. Selective reduction of the nitro group using Fe/dil.HCl is achieved for the 4‐nitro derivative but this is not effective when ethoxymethylenemalononitrile is used to trap the amine. For 5‐nitroimidazole studies the N‐vinyl substituent is kept masked as a 2‐chloroethyl group, which remains unchanged during catalytic reduction of the nitro function (Pd/C), and is revealed by HCl elimination at a later stage. In this way, the 1‐deazapurine 13 and the tricyclic derivative 14 have been prepared.
    DOI:
    10.1002/jhet.5570410508
点击查看最新优质反应信息