62849-10-9

Basic information

• Product Name: α-[(2,4-Dimethoxyphenyl)methyl]-β,3,4-trimethoxybenzeneethanol
• Synonyms: α-[(2,4-Dimethoxyphenyl)methyl]-β,3,4-trimethoxybenzeneethanol
• CAS NO: 62849-10-9
• Molecular Formula: C20H26O6
• Molecular Weight: 362.41684
• Mol File: 62849-10-9.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: α-[(2,4-Dimethoxyphenyl)methyl]-β,3,4-trimethoxybenzeneethanol(CAS DataBase Reference)
• NIST Chemistry Reference: α-[(2,4-Dimethoxyphenyl)methyl]-β,3,4-trimethoxybenzeneethanol(62849-10-9)
• EPA Substance Registry System: α-[(2,4-Dimethoxyphenyl)methyl]-β,3,4-trimethoxybenzeneethanol(62849-10-9)

Safety Data

• Hazardous Substances Data: 62849-10-9(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 67-56-1 methanol 
• 490-49-3 fisetinidol 

Relevant articles and documents

Flavonoid synthesis based on photolysis of flavan-3-ols, 3-hydroxyflavanones, and 2-benzylbenzofuranones

Irradiation of flavan-3-ols, 3-hydroxyflavanones, and 2-benzylbenzofuranones in methanol leads mainly to photochemical opening of the heterocyclic ring, or to its complete photofragmentation, the products being trapped by reaction with the solvent. Fission of exocyclic C-O bonds also occurs, accompanied by intramolecular rearrangements. The course of these reactions is often dependent on the position and nature of substituents. The conversions provide novel routes to 1,3-diaryl-1-methoxypropan-2-ols, 1,3-diaryl-2,2-dimethoxypropan-1-ones, cis-3-methoxyflavanones, isoflavones, flavanones, and trans-chalcones, and hence to α-hydroxychalcones, cis- and trans-α-methoxychalcones, and 2-methoxy-2-(α-methoxybenzyl)benzofuranones.