76672-92-9

Basic information

• Product Name: 3-(3,4-dimethoxybenzyl)-7-methoxy-4-chromanone
• Synonyms: 3-(3,4-dimethoxybenzyl)-7-methoxy-4-chromanone
• CAS NO: 76672-92-9
• Molecular Weight: 328.365
• Mol File: 76672-92-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-(3,4-dimethoxybenzyl)-7-methoxy-4-chromanone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3,4-dimethoxybenzyl)-7-methoxy-4-chromanone(76672-92-9)
• EPA Substance Registry System: 3-(3,4-dimethoxybenzyl)-7-methoxy-4-chromanone(76672-92-9)

Safety Data

• Hazardous Substances Data: 76672-92-9(Hazardous Substances Data)

Upstream product

• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 76672-90-7 3-(3,4-dimethoxyphenyl)-1-(2-hydroxy-4-methoxyphenyl)-1-propanone 
• 57601-14-6 2'-hydroxy-3,4,4'-trimethoxychalcone 
• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 
• 50-00-0 formaldehyd 
• 105245-59-8 2'-Hydroxy-3,4,4'-trimethoxy-α-hydroxymethyldihydrochalcone 
• 91100-83-3 3-(3,4-dimethoxybenzyl)-7-methoxy-4H-chromen-4-one 
• 75-11-6 diiodomethane 
• 186581-53-3 diazomethane 
• 102067-88-9 3-deoxysappanone B 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 111254-23-0 (3R,4S)-3,4-dihydroxy-3-(3,4-dimethoxybenzyl)-7-methoxychroman 
• 113187-32-9 (3R,4R)-3-(3,4-Dimethoxy-benzyl)-4,7-dimethoxy-chroman-3-ol 
• 111254-24-1 (3R,4R)-3,4-dihydroxy-3-(3,4-dimethoxybenzyl)-7-methoxychroman 
• 113122-58-0 (R)-(-)-O-trimethylsappanone B 

Relevant articles and documents

An improved synthesis of homoisoflavanones

2′-Hydroxydihydrochalcones i.e. 1-(2-hydroxyphenyl)-3- phenylpropanones having different oxygenation patterns in ring-A and ring-B, on refluxing with paraformaldehyde powder and aqueous diethylamine in ethanol give the corresponding homoisoflavanones in excellent yields.

Homoisoflavonoids and Related Compounds. IV. Absolute Configurations of Homoisoflavonoids from Caesalpinia sappan L.

The absolute configuration of the homoisoflavonoidal components, 4-O-methylsappanol, 4-O-methylepisappanol, sappanone B, 3-deoxysappanone B and 3'-deoxysappanone B, from Caesalpinia sappan L. were determined on the basis of chemical transformations and the optical properties.Keywords - Caesalpinia sappan; Leguminosae; Sappan Lignum; heartwood; homoisoflavonoid; absolute configuration

A New Biogenetic Approach for the Synthesis of Homoisoflavanones

2'-Hydroxydihydrochalkones on refluxing with methylene iodide in acetone medium in the presence of anhydrous potassium carbonate have been found to yield bi(dihydrochalkonyloxy)methanes and homoisoflavanones.