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

N-benzyl-4-[benzyl-[4-[benzyl-[4-[benzyl-(4-nitronaphthalene-1-carbonyl)amino]naphthalene-1-carbonyl]amino]naphthalene-1-carbonyl]amino]-N-phenylnaphthalene-1-carboxamide | 1255217-70-9

中文名称
——
中文别名
——
英文名称
N-benzyl-4-[benzyl-[4-[benzyl-[4-[benzyl-(4-nitronaphthalene-1-carbonyl)amino]naphthalene-1-carbonyl]amino]naphthalene-1-carbonyl]amino]-N-phenylnaphthalene-1-carboxamide
英文别名
——
N-benzyl-4-[benzyl-[4-[benzyl-[4-[benzyl-(4-nitronaphthalene-1-carbonyl)amino]naphthalene-1-carbonyl]amino]naphthalene-1-carbonyl]amino]-N-phenylnaphthalene-1-carboxamide化学式
CAS
1255217-70-9
化学式
C78H57N5O6
mdl
——
分子量
1160.34
InChiKey
PZMKLVALTMVKEU-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):
    16.8
  • 重原子数:
    89
  • 可旋转键数:
    16
  • 环数:
    13.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    127
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    N-benzyl-N-(4-(benzyl(4-(benzyl(phenyl)carbamoyl)naphthalen-1-yl)carbamoyl)naphthalen-1-yl)-4-(4-nitro-1-naphthamido)-1-naphthamide 、 溴甲苯 在 sodium hydride 作用下, 以 四氢呋喃 为溶剂, 反应 3.25h, 以23%的产率得到N-benzyl-4-[benzyl-[4-[benzyl-[4-[benzyl-(4-nitronaphthalene-1-carbonyl)amino]naphthalene-1-carbonyl]amino]naphthalene-1-carbonyl]amino]-N-phenylnaphthalene-1-carboxamide
    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
点击查看最新优质反应信息

文献信息

  • Conformational studies of tertiary oligo-m-benzanilides and oligo-p-benzanilides in solution
    作者:Laurent Chabaud、Jonathan Clayden、Madeleine Helliwell、Abigail Page、James Raftery、Lluís Vallverdú
    DOI:10.1016/j.tet.2010.06.037
    日期:2010.8
    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.
查看更多