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(S)-2-methyl-1-(1-octyl-1H-benzo[d]imidazol-2-yl)propan-1-amine | 1448513-17-4

中文名称
——
中文别名
——
英文名称
(S)-2-methyl-1-(1-octyl-1H-benzo[d]imidazol-2-yl)propan-1-amine
英文别名
——
(S)-2-methyl-1-(1-octyl-1H-benzo[d]imidazol-2-yl)propan-1-amine化学式
CAS
1448513-17-4
化学式
C19H31N3
mdl
——
分子量
301.475
InChiKey
ZBKLNGRFMPHDCV-SFHVURJKSA-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):
    5.05
  • 重原子数:
    22.0
  • 可旋转键数:
    9.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.63
  • 拓扑面积:
    43.84
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

上下游信息

  • 下游产品
    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:
    描述:
    (S)-2-methyl-1-(1-octyl-1H-benzo[d]imidazol-2-yl)propan-1-amine间苯二异氰酸酯N,N-二异丙基乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 9.0h, 以0.08 g的产率得到1-[(1S)-2-methyl-1-(1-octylbenzimidazol-2-yl)propyl]-3-[3-[[(1S)-2-methyl-1-(1-octylbenzimidazol-2-yl)propyl]carbamoylamino]phenyl]urea
    参考文献:
    名称:
    l-Valine derived benzimidazole based bis-urea in enantioselective fluorescence sensing of L-tartrate
    摘要:
    L-Valine derived benzimidazole based bis-urea 1 has been designed and synthesized. The bis-urea 1 is found to act as enantioselective chemosensor for tartrate. The sensor shows greater fluorescence response for L-tartrate in DMSO. The enantiomeric fluorescence difference ratio (ef) has been determined to be 2.46. In comparison, less steric receptor 2 exhibits a marginal preference for D-tartrate over the L-tartrate in DMSO and validates the steric role of the substituents around the benzimidazole motif in 1 toward enantioselective recognition of tartrate. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.06.087
  • 作为产物:
    参考文献:
    名称:
    l-Valine derived benzimidazole based bis-urea in enantioselective fluorescence sensing of L-tartrate
    摘要:
    L-Valine derived benzimidazole based bis-urea 1 has been designed and synthesized. The bis-urea 1 is found to act as enantioselective chemosensor for tartrate. The sensor shows greater fluorescence response for L-tartrate in DMSO. The enantiomeric fluorescence difference ratio (ef) has been determined to be 2.46. In comparison, less steric receptor 2 exhibits a marginal preference for D-tartrate over the L-tartrate in DMSO and validates the steric role of the substituents around the benzimidazole motif in 1 toward enantioselective recognition of tartrate. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.06.087
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