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N-(2-溴-4-甲基苯基)-2-萘酰胺 | 416874-40-3

中文名称
N-(2-溴-4-甲基苯基)-2-萘酰胺
中文别名
——
英文名称
N-(2-bromo-4-methylphenyl)-2-naphthamide
英文别名
N-(2-bromo-4-methylphenyl)naphthalene-2-carboxamide
N-(2-溴-4-甲基苯基)-2-萘酰胺化学式
CAS
416874-40-3
化学式
C18H14BrNO
mdl
——
分子量
340.219
InChiKey
PMAXLXLKRWIBNP-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

物化性质

  • 熔点:
    116-121 °C(Solvent: Hexane)
  • 沸点:
    400.5±38.0 °C(Predicted)
  • 密度:
    1.448±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    21
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    1

SDS

SDS:d57b6cd45fb795514df27fce165f2fb8
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反应信息

  • 作为反应物:
    描述:
    N-(2-溴-4-甲基苯基)-2-萘酰胺四甲基乙二胺 、 copper(II) bis(trifluoromethanesulfonate) 作用下, 以 为溶剂, 以65%的产率得到6-methyl-2-(2-naphthyl)benzo[d]oxazole
    参考文献:
    名称:
    Copper-catalysed intramolecular O-arylation of aryl chlorides and bromides: a straightforward approach to benzo[d]oxazoles in water
    摘要:
    A general, efficient and more sustainable protocol for the copper-catalysed intramolecular O-arylation of o'- haloanilides leading to the benzo[d]oxazole core is reported. Remarkably, the optimised conditions allowed for the use of inexpensive and easily available aryl chlorides as arylating agents. Moreover, all reactions were carried out employing exclusively water as the solvent, rendering the methodology presented herein highly valuable from both environmental and economic points of view. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2007.08.013
  • 作为产物:
    描述:
    2-萘甲酸吡啶氯化亚砜 作用下, 以 二氯甲烷甲苯 为溶剂, 反应 3.0h, 生成 N-(2-溴-4-甲基苯基)-2-萘酰胺
    参考文献:
    名称:
    Copper-catalysed intramolecular O-arylation of aryl chlorides and bromides: a straightforward approach to benzo[d]oxazoles in water
    摘要:
    A general, efficient and more sustainable protocol for the copper-catalysed intramolecular O-arylation of o'- haloanilides leading to the benzo[d]oxazole core is reported. Remarkably, the optimised conditions allowed for the use of inexpensive and easily available aryl chlorides as arylating agents. Moreover, all reactions were carried out employing exclusively water as the solvent, rendering the methodology presented herein highly valuable from both environmental and economic points of view. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2007.08.013
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文献信息

  • Copper-catalysed intramolecular O-arylation of aryl chlorides and bromides: a straightforward approach to benzo[d]oxazoles in water
    作者:Nekane Barbero、Mónica Carril、Raul SanMartin、Esther Domínguez
    DOI:10.1016/j.tet.2007.08.013
    日期:2007.10
    A general, efficient and more sustainable protocol for the copper-catalysed intramolecular O-arylation of o'- haloanilides leading to the benzo[d]oxazole core is reported. Remarkably, the optimised conditions allowed for the use of inexpensive and easily available aryl chlorides as arylating agents. Moreover, all reactions were carried out employing exclusively water as the solvent, rendering the methodology presented herein highly valuable from both environmental and economic points of view. (c) 2007 Elsevier Ltd. All rights reserved.
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