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5-(6-bromo-2-methylbenzo[b]thiophen-3-yl)-N-methoxy-N-methyl-5-oxopentanamide | 1422739-49-8

中文名称
——
中文别名
——
英文名称
5-(6-bromo-2-methylbenzo[b]thiophen-3-yl)-N-methoxy-N-methyl-5-oxopentanamide
英文别名
5-(6-bromo-2-methyl-1-benzothiophen-3-yl)-N-methoxy-N-methyl-5-oxopentanamide
5-(6-bromo-2-methylbenzo[b]thiophen-3-yl)-N-methoxy-N-methyl-5-oxopentanamide化学式
CAS
1422739-49-8
化学式
C16H18BrNO3S
mdl
——
分子量
384.294
InChiKey
MHHHBRWRVRLENV-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):
    3.5
  • 重原子数:
    22
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    74.8
  • 氢给体数:
    0
  • 氢受体数:
    4

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:
    描述:
    5-(6-bromo-2-methylbenzo[b]thiophen-3-yl)-N-methoxy-N-methyl-5-oxopentanamide 、 tributylstannylferrocene 在 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloridecopper(II) oxide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 0.42h, 以64%的产率得到5-(6-ferrocenyl-2-methylbenzo[b]thiophen-3-yl)-N-methoxy-N-methyl-5-oxopentanamide
    参考文献:
    名称:
    Synthesis of a ferrocene-functionalized unsymmetrical benzo[b]thienyl-thienylethene photoswitch with a cyclopentene core
    摘要:
    A new and potentially general synthetic route toward unsymmetrical benzo[b]thienyl-thienylethene compounds is described, with specific focus on conjugation of a ferrocene to the benzo[b]thiophene subunit. The route proceeds in an overall yield of 17%. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.01.033
  • 作为产物:
    描述:
    6-溴-2-甲基苯并[B]噻吩 在 aluminum (III) chloride 作用下, 以 二氯甲烷 为溶剂, 反应 19.25h, 生成 5-(6-bromo-2-methylbenzo[b]thiophen-3-yl)-N-methoxy-N-methyl-5-oxopentanamide
    参考文献:
    名称:
    Synthesis of a ferrocene-functionalized unsymmetrical benzo[b]thienyl-thienylethene photoswitch with a cyclopentene core
    摘要:
    A new and potentially general synthetic route toward unsymmetrical benzo[b]thienyl-thienylethene compounds is described, with specific focus on conjugation of a ferrocene to the benzo[b]thiophene subunit. The route proceeds in an overall yield of 17%. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.01.033
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文献信息

  • Synthesis of a ferrocene-functionalized unsymmetrical benzo[b]thienyl-thienylethene photoswitch with a cyclopentene core
    作者:Nathaniel B. Zuckerman、Xiongwu Kang、Shaowei Chen、Joseph P. Konopelski
    DOI:10.1016/j.tetlet.2013.01.033
    日期:2013.3
    A new and potentially general synthetic route toward unsymmetrical benzo[b]thienyl-thienylethene compounds is described, with specific focus on conjugation of a ferrocene to the benzo[b]thiophene subunit. The route proceeds in an overall yield of 17%. (C) 2013 Elsevier Ltd. All rights reserved.
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