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N,N-diethyl-3-allyl-4,6-dimethoxybenzo[b]thiophene-2-carboxamide | 530101-67-8

中文名称
——
中文别名
——
英文名称
N,N-diethyl-3-allyl-4,6-dimethoxybenzo[b]thiophene-2-carboxamide
英文别名
N,N-diethyl-4,6-dimethoxy-3-prop-2-enyl-1-benzothiophene-2-carboxamide
N,N-diethyl-3-allyl-4,6-dimethoxybenzo[b]thiophene-2-carboxamide化学式
CAS
530101-67-8
化学式
C18H23NO3S
mdl
——
分子量
333.452
InChiKey
WCOBBXUWZDWKTK-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):
    4.5
  • 重原子数:
    23
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    67
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    N,N-diethyl-3-allyl-4,6-dimethoxybenzo[b]thiophene-2-carboxamide盐酸 作用下, 以 为溶剂, 反应 60.0h, 生成 5,7-Dihydroxy-3-methyl-3,4-dihydro-benzo[4,5]thieno[2,3-c]pyran-1-one
    参考文献:
    名称:
    Application of directed metallation in synthesis. Part 3: Studies in the synthesis of (±)-semivioxanthin and its analogues
    摘要:
    The synthesis of several analogues of (+/-)-semivioxanthin including five thiophene analogues, using directed metalation are reported. The strategy consisted of the synthesis of functionalized naphthalene or benzo[b]thiophene as building blocks followed by annelation of the pyrone. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(02)01599-5
  • 作为产物:
    参考文献:
    名称:
    Application of directed metallation in synthesis. Part 3: Studies in the synthesis of (±)-semivioxanthin and its analogues
    摘要:
    The synthesis of several analogues of (+/-)-semivioxanthin including five thiophene analogues, using directed metalation are reported. The strategy consisted of the synthesis of functionalized naphthalene or benzo[b]thiophene as building blocks followed by annelation of the pyrone. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(02)01599-5
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文献信息

  • Application of directed metallation in synthesis. Part 3: Studies in the synthesis of (±)-semivioxanthin and its analogues
    作者:Sukanta Kamila、Chandrani Mukherjee、Sasanka S Mondal、Asish De
    DOI:10.1016/s0040-4020(02)01599-5
    日期:2003.2
    The synthesis of several analogues of (+/-)-semivioxanthin including five thiophene analogues, using directed metalation are reported. The strategy consisted of the synthesis of functionalized naphthalene or benzo[b]thiophene as building blocks followed by annelation of the pyrone. (C) 2003 Elsevier Science Ltd. All rights reserved.
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