(E)-3',6-dimethoxyaurone

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 橙酮类黄酮
• 英文名称: (E)-3',6-dimethoxyaurone
• 英文别名: 2-[(3-methoxyphenyl)methylene]-6-methoxy-3(2H)-benzofuranone；6-methoxy-2-[(3-methoxyphenyl)methylidene]-1-benzofuran-3-one
• 化学式: C₁₇H₁₄O₄
• 分子量: 282.296
• InChiKey: VGYKFEDOWJOOCJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  21
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  44.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  6-甲氧基-3-苯并呋喃酮 、 3-甲氧基苯甲醛 在 盐酸 作用下， 以 溶剂黄146 为溶剂， 反应 16.0h， 以510 mg的产率得到(E)-3',6-dimethoxyaurone
  参考文献：
  名称：

  Proximity effects in the electron impact mass spectra of aurones and related compounds

  摘要：

  AbstractThe principal ions in the electron impact mass spectra of a series of 6‐methoxyaurones have been shown to be due to four separate reactions associated with proximity effects involving the phenyl group and the coumaran‐one residue. A detailed study with labelled derivatives has been supplemented by a study of the vinylogue 2‐cinnamylidene‐6‐methoxycoumaran‐3‐one and compounds in which the aurone phenyl group has been replaced by α‐naphthyl, β‐naphthyl and 9‐anthryl.

  DOI：

  10.1002/oms.1210151102

文献信息

• Benzofuranone derivatives and a method for producing them
  申请人：Snow Brand Milk Products Co., Ltd.

  公开号：US06143779A1

  公开（公告）日：2000-11-07

  The present invention provides new benzofuranone derivatives and a method for producing the derivatives useful for a therapeutic agent for preventing and/or treating hormone dependent diseases. The present invention is a new benzofuranone derivative represented by a particular general formula (I). ##STR1## In the production, a particular benzofuranone compound and a particular benzaldehyde are reacted.

  本发明提供了新的苯并呋喃酮衍生物及其制备方法，用于预防和/或治疗激素依赖性疾病的治疗剂。本发明是一种由特定通式（I）表示的新苯并呋喃酮衍生物。在制备中，特定的苯并呋喃酮化合物和特定的苯甲醛反应。
• Proximity effects in the electron impact mass spectra of aurones and related compounds
  作者：R. J. Goldsack、J. S. Shannon

  DOI：10.1002/oms.1210151102

  日期：1980.11

  AbstractThe principal ions in the electron impact mass spectra of a series of 6‐methoxyaurones have been shown to be due to four separate reactions associated with proximity effects involving the phenyl group and the coumaran‐one residue. A detailed study with labelled derivatives has been supplemented by a study of the vinylogue 2‐cinnamylidene‐6‐methoxycoumaran‐3‐one and compounds in which the aurone phenyl group has been replaced by α‐naphthyl, β‐naphthyl and 9‐anthryl.