2-methyl-5,6,7-trimethoxychromone | 63044-77-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 英文名称: 2-methyl-5,6,7-trimethoxychromone
• 英文别名: 5,6,7-Trimethoxy-2-methylchromone；5,6,7-trimethoxy-2-methyl-chromen-4-one；5,6,7-Trimethoxy-2-methyl-chromen-4-on；5,6,7-Trimethoxy-2-methyl-4H-1-benzopyran-4-one；5,6,7-trimethoxy-2-methylchromen-4-one
• CAS: 63044-77-9
• 化学式: C₁₃H₁₄O₅
• 分子量: 250.251
• InChiKey: YNKGEYCEQIJBFT-UHFFFAOYSA-N

物化性质

• 熔点：
  100 °C(Solv: water (7732-18-5))
• 沸点：
  402.6±45.0 °C(Predicted)
• 密度：
  1.208±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  54
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-methyl-5,6,7-trimethoxychromone 在 sodium methylate 、 lithium diisopropyl amide 作用下， 以 甲醇 为溶剂， 反应 5.0h， 生成 5,6,7-Trimethoxy-2-<2-(3,5-dimethoxyphenyl)ethenyl>-3-methylchromone
  参考文献：
  名称：

  Synthesis of highly functionalized flavones and chromones using cycloacylation reactions and C-3 functionalization. A total synthesis of hormothamnione

  摘要：

  DOI：

  10.1021/jo00301a027
• 作为产物：
  描述：

  3,4,5-三甲氧基苯酚 在 甲烷磺酸 、 phosphorus pentoxide 、 potassium carbonate 作用下， 以 丙酮 为溶剂， 反应 6.0h， 生成 2-methyl-5,6,7-trimethoxychromone
  参考文献：
  名称：

  Synthesis of highly functionalized flavones and chromones using cycloacylation reactions and C-3 functionalization. A total synthesis of hormothamnione

  摘要：

  DOI：

  10.1021/jo00301a027

文献信息

• Three chromones from bulbs of Pancratium biflorum
  作者：Shibnath Ghosal、Shripati Singh、Mahendra P. Bhagat、Yatendra Kumar

  DOI：10.1016/0031-9422(80)85074-6

  日期：1980.1

  Abstract Two polyoxygenated chromones, 5,7-dihydroxy-2-methylchromone (1) and 5,6-dihydroxy-7- methoxy-2-methylchromone(2), and a glucosyloxychromone, 7

  摘要 两种多氧化色酮，5,7-二羟基-2-甲基色酮 (1) 和 5,6-二羟基-7-甲氧基-2-甲基色酮 (2)，以及一种葡糖氧基色酮，7
• Synthesis, biological evaluation and molecular docking studies of stellatin derivatives as cyclooxygenase (COX-1, COX-2) inhibitors and anti-inflammatory agents
  作者：Raju Gautam、Sanjay M. Jachak、Vivek Kumar、C. Gopi Mohan

  DOI：10.1016/j.bmcl.2011.01.116

  日期：2011.3

  Stellatin (4), isolated from Dysophylla stellata is a cyclooxygenase (COX) inhibitor. The present study reports the synthesis and biological evaluation of new stellatin derivatives for COX-1, COX-2 inhibitory and anti-inflammatory activities. Eight derivatives showed more pronounced COX-2 inhibition than stellatin and, 17 and 21 exhibited the highest COX-2 inhibition. They also exhibited the significant anti-inflammatory activity in TPA-induced mouse ear edema assay and their anti-inflammatory effects were more than that of stellatin and indomethacin at 0.5 mg/ear. The derivatives were further evaluated for antioxidant activity wherein 16 and 17 showed potent free radical scavenging activity against DPPH and ABTS radicals. Molecular docking study revealed the binding orientations of stellatin and its derivatives into the active sites of COX-1 and COX-2 and thereby helps to design the potent inhibitors. (C) 2011 Elsevier Ltd. All rights reserved.
• Chakravorty et al., Proceedings - Indian Academy of Sciences, Section A, 1952, # 35, p. 34,41
  作者：Chakravorty et al.

  DOI：——

  日期：——
• Furo-chromones and -Coumarins. IX. Reactions of Khellol Glucoside, Visnagin and Bergapten
  作者：Alexander Schönberg、Nasry Badran、Nicolas A. Starkowsky

  DOI：10.1021/ja01609a066

  日期：1955.2
• MCGARRY, LYNDA W.;DETTY, MICHAEL R., J. ORG. CHEM., 55,(1990) N4, C. 4349-4356
  作者：MCGARRY, LYNDA W.、DETTY, MICHAEL R.

  DOI：——

  日期：——