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phenyl 5,6-dimethoxy-3-phenoxybenzothiophene-2-carboxylate | 138835-18-4

中文名称
——
中文别名
——
英文名称
phenyl 5,6-dimethoxy-3-phenoxybenzothiophene-2-carboxylate
英文别名
phenyl 5,6-dimethoxy-3-phenoxy-1-benzothiophene-2-carboxylate
phenyl 5,6-dimethoxy-3-phenoxybenzo<b>thiophene-2-carboxylate化学式
CAS
138835-18-4
化学式
C23H18O5S
mdl
——
分子量
406.459
InChiKey
DKUYFVGRCSFDPL-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

  • 沸点:
    552.8±50.0 °C(Predicted)
  • 密度:
    1.290±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.93
  • 重原子数:
    29.0
  • 可旋转键数:
    6.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    53.99
  • 氢给体数:
    0.0
  • 氢受体数:
    6.0

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:
    phenyl 5,6-dimethoxy-3-phenoxybenzothiophene-2-carboxylatesodium hydroxide 作用下, 以 甲醇 为溶剂, 反应 5.0h, 以84%的产率得到5,6-dimethoxy-3-phenoxybenzothiophene-2-carboxylic acid
    参考文献:
    名称:
    Novel benzothiophene-, benzofuran-, and naphthalenecarboxamidotetrazoles as potential antiallergy agents
    摘要:
    The synthesis and antiallergic activity of a series of novel benzothiophene-, benzofuran-, and naphthalenecarbox-amidotetrazoles are described. A number of the compounds inhibit the release of histamine from anti-IgE stimulated basophils obtained from allergic donors. Optimal inhibition is exhibited in benzothiophenes with a 3-alkoxy substituent in combination with a 5-methoxy, 6-methoxy, or a 5,6-dimethoxy group. Compounds 13c (CI-959) also inhibited respiratory burst of human neutrophils and the release of mediators from anti-IgE-stimulated human chopped lung.
    DOI:
    10.1021/jm00083a023
  • 作为产物:
    描述:
    苯酚三乙胺 作用下, 以 二甲基亚砜丙酮 为溶剂, 反应 7.0h, 生成 phenyl 5,6-dimethoxy-3-phenoxybenzothiophene-2-carboxylate
    参考文献:
    名称:
    Novel benzothiophene-, benzofuran-, and naphthalenecarboxamidotetrazoles as potential antiallergy agents
    摘要:
    The synthesis and antiallergic activity of a series of novel benzothiophene-, benzofuran-, and naphthalenecarbox-amidotetrazoles are described. A number of the compounds inhibit the release of histamine from anti-IgE stimulated basophils obtained from allergic donors. Optimal inhibition is exhibited in benzothiophenes with a 3-alkoxy substituent in combination with a 5-methoxy, 6-methoxy, or a 5,6-dimethoxy group. Compounds 13c (CI-959) also inhibited respiratory burst of human neutrophils and the release of mediators from anti-IgE-stimulated human chopped lung.
    DOI:
    10.1021/jm00083a023
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