2-羟基-1-甲氧基呫吨酮 | 16302-46-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 中文名称: 2-羟基-1-甲氧基呫吨酮
• 英文名称: 2-Hydroxy-1-methoxy-xanthen-9-one
• 英文别名: 2-hydroxy-1-methoxyxanthone；7-hydroxy-8-methoxyxanthone；1-methoxy-2-hydroxyxanthone；2-hydroxy-1-methoxyxanthen-9-one
• CAS: 16302-46-8
• 化学式: C₁₄H₁₀O₄
• 分子量: 242.231
• InChiKey: ATPZBKJDXXSOFC-UHFFFAOYSA-N

物化性质

• 熔点：
  169-171 °C
• 沸点：
  452.6±45.0 °C(Predicted)
• 密度：
  1.375±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  18
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  55.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  1-Formyl-2-hydroxy-9-xanthenon 在 吡啶 、 sodium hydroxide 、 双氧水 作用下， 生成 2-羟基-1-甲氧基呫吨酮
  参考文献：
  名称：

  Davies et al., Journal of the Chemical Society, 1958, p. 1790,1793

  摘要：

  DOI：

文献信息

• Intramolecular Anionic Friedel-Crafts Equivalents. A General Regiospecific Route to Substituted and Naturally Occurring Xanthen-9-ones
  作者：O. Familoni、Ileana Ionica、Justin Bower、Victor Snieckus

  DOI：10.1055/s-1997-1533

  日期：1997.9

  An LDA-induced regiospecific and general conversion of diaryl ether 2-carboxamides 4 into substituted xanthones 5, including natural products, 2-hydroxy-1-methoxyxanthone (8) and 6-deoxy-jacareubin (14), is described.

  报道了一种由线性判别分析诱导的、对二芳基醚2-羧酰胺4的区域特异性及普遍性转化，生成取代咕吨酮5，包括天然产物2-羟基-1-甲氧基咕吨酮(8)和6-脱氧雅卡尔宾(14)。
• The synthesis of xanthones, xanthenediones, and spirobenzofurans: Their antibacterial and antifungal activity
  作者：Justin J. Omolo、Myron M. Johnson、Sandy F. van Vuuren、Charles B. de Koning

  DOI：10.1016/j.bmcl.2011.09.088

  日期：2011.12

  Exposure of the phenol, (5-bromo-2-hydroxyphenyl)(2,4,5-trimethoxyphenyl)methanone 18 to ceric ammonium nitrate (CAN) resulted in the formation of 7-bromo-3,4a-dimethoxy-2H-xanthene-2,9( 4aH)-dione 19 and 5-bromo-2',5'-dimethoxy-3H-spiro[benzofuran-2,1'-cyclohexa[2,5]diene]-3,4'-dione 20. The brominated spirobenzofuran 20 was then subjected to Suzuki-Miyaura reactions to give six derivatives 22a-f. These compounds, related diones and xanthones displayed mostly noteworthy antimicrobial activity, particularly towards the yeasts Cryptococcus neoformans and Candida albicans. Diones 15 and 30 displayed significant activity (7.8 mu g/mL) against C. albicans and C. neoformans, respectively. Furthermore, dione 10 displayed the most significant activity (3.6 mu g/mL) against both yeasts. (C) 2011 Elsevier Ltd. All rights reserved.
• Davies et al., Journal of the Chemical Society, 1958, p. 1790,1793
  作者：Davies et al.

  DOI：——

  日期：——