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4-amino-N-benzyl-N-phenyl-1-naphthamide | 1271741-24-2

中文名称
——
中文别名
——
英文名称
4-amino-N-benzyl-N-phenyl-1-naphthamide
英文别名
——
4-amino-N-benzyl-N-phenyl-1-naphthamide化学式
CAS
1271741-24-2
化学式
C24H20N2O
mdl
——
分子量
352.436
InChiKey
CJKJZTRYOVMZKS-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):
    5.27
  • 重原子数:
    27.0
  • 可旋转键数:
    4.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.04
  • 拓扑面积:
    46.33
  • 氢给体数:
    1.0
  • 氢受体数:
    2.0

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
  • 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:
    4-amino-N-benzyl-N-phenyl-1-naphthamide4-nitro-1-nathphoyl chloride二氯甲烷 为溶剂, 以97%的产率得到N-benzyl-4-(4-nitro-1-naphthamido)-N-phenyl-1-naphthamide
    参考文献:
    名称:
    Conformational studies of tertiary oligo-m-benzanilides and oligo-p-benzanilides in solution
    摘要:
    A series of oligo-m- and p-benzanilides were made and their conformations in solution were studied by NMR. In most cases, conformational mixtures were observed as soon as three or more monomers were incorporated into the oligomer. Some crystal structures were obtained, which indicated that helical conformations were adopted in the solid state. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2010.06.037
  • 作为产物:
    描述:
    N-benzyl-4-nitro-N-phenyl-1-naphthamidetin(II) chloride dihdyrate 作用下, 以 乙酸乙酯 为溶剂, 以83%的产率得到4-amino-N-benzyl-N-phenyl-1-naphthamide
    参考文献:
    名称:
    Conformational studies of tertiary oligo-m-benzanilides and oligo-p-benzanilides in solution
    摘要:
    A series of oligo-m- and p-benzanilides were made and their conformations in solution were studied by NMR. In most cases, conformational mixtures were observed as soon as three or more monomers were incorporated into the oligomer. Some crystal structures were obtained, which indicated that helical conformations were adopted in the solid state. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2010.06.037
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