3-（3'，4'，5'-三甲氧基苯基）-1,2-丙二醇 | 54306-10-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 中文名称: 3-（3'，4'，5'-三甲氧基苯基）-1,2-丙二醇
• 英文名称: p-methoxytodadiol
• 英文别名: 3-(3',4',5'-trimethoxyphenyl)-1,2-propanediol；3-(3,4,5-trimethoxy-phenyl)-propane-1,2-diol；3-(3,4,5-Trimethoxy-phenyl)-propan-1,2-diol；3-(3,4,5-Trimethoxyphenyl)propane-1,2-diol
• CAS: 54306-10-4
• 化学式: C₁₂H₁₈O₅
• 分子量: 242.272
• InChiKey: SNDFRVPKIVPGED-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.4
• 重原子数：
  17
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  68.2
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  3-（3'，4'，5'-三甲氧基苯基）-1,2-丙二醇 在 lead(IV) acetate 、 苯 作用下， 生成 3,4,5-三甲氧基苯乙醛
  参考文献：
  名称：

  THE SYNTHESIS OF 3,4,5-TRIMETHOXYPHENYLACETALDEHYDE

  摘要：

  无法使用。

  DOI：

  10.1139/v56-111
• 作为产物：
  描述：

  榄香素 在 potassium permanganate 作用下， 生成 3-（3'，4'，5'-三甲氧基苯基）-1,2-丙二醇
  参考文献：
  名称：

  THE SYNTHESIS OF 3,4,5-TRIMETHOXYPHENYLACETALDEHYDE

  摘要：

  无法使用。

  DOI：

  10.1139/v56-111

文献信息

• LEWIS X DERIVATIVE AND PROCESS FOR PRODUCING THE SAME
  申请人：SUMITOMO PHARMACEUTICALS COMPANY, LIMITED

  公开号：EP0801071A1

  公开（公告）日：1997-10-15

  A novel oligosaccharide derivative having a cell adhesion inhibitory activity and represented by structural formula (I).

  一种具有细胞粘附抑制活性的新型寡糖衍生物，由结构式（I）表示。
• Structure–activity relationship of chemical defenses from the freshwater plant Micranthemum umbrosum
  作者：Amy L. Lane、Julia Kubanek

  DOI：10.1016/j.phytochem.2006.05.007

  日期：2006.6

  Vascular plants produce a variety of molecules of phenylpropanoid biosynthetic origin, including lignoids. Recent investigations indicated that in freshwater plants, some of these natural products function as chemical defenses against generalist consumers such as crayfish. Certain structural features are shared among several of these anti-herbivore compounds, including phenolic, methoxy, methylenedioxy, and lactone functional groups. To test the relative importance of various functional groups in contributing to the feeding deterrence of phenylpropanoid-based natural products, we compared the feeding behavior of crayfish offered artificial diets containing analogs of elemicin (1) and beta-apopicropodophyllin (2), chemical defenses of the freshwater macrophyte Micranthemum umbrosum. Both allyl and methoxy moieties of 1 contributed to feeding deterrence. Disruption of the lactone moiety of 2 reduced its deterrence. Finally, feeding assays testing effects of 1 and 2 at multiple concentrations established that these two natural products interact additively in deterring crayfish feeding. (c) 2006 Elsevier Ltd. All rights reserved.
• THE SYNTHESIS OF 3,4,5-TRIMETHOXYPHENYLACETALDEHYDE
  作者：J. G. Duff、J. M. Pepper

  DOI：10.1139/v56-111

  日期：1956.6.1

  not available

  无法使用。