27181-65-3

Basic information

• Product Name: (E)-5,7-dimethoxy-3-(4-methoxybenzylidene)-4-chromanone
• CAS NO: 27181-65-3
• Molecular Weight: 326.349
• Mol File: 27181-65-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-5,7-dimethoxy-3-(4-methoxybenzylidene)-4-chromanone(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-5,7-dimethoxy-3-(4-methoxybenzylidene)-4-chromanone(27181-65-3)
• EPA Substance Registry System: (E)-5,7-dimethoxy-3-(4-methoxybenzylidene)-4-chromanone(27181-65-3)

Safety Data

• Hazardous Substances Data: 27181-65-3(Hazardous Substances Data)

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 1013631-83-8 C₁₂H₁₃BrO₃ 
• 115240-92-1 methyl 2-[hydroxy(4-methoxyphenyl)methyl]prop-2-enoate 
• 59887-91-1 5,7-dimethoxy-4H-chromen-4-one 
• 90-24-4 2-hydroxy-4,6-dimethoxyacetophenone 
• 854678-45-8 β-(3,5-dimethoxyphenoxy)propionic acid 
• 54107-66-3 5,7-dimethoxy-4-chromanone 
• 500-99-2 3,5-dimethoxyphenol 

Downstream Products

• 3791-75-1 2'-hydroxy-4,4',6'-trimethoxydihydrochalcone 
• 246244-10-0 rac-5,7-dimethoxy-3-(4-methoxybenzyl)-chroman-4-one 
• 22395-14-8 3-methyl-5,7,4′-trimethoxyflavone 
• 34811-77-3 3-(4-methyloxybenzyl)-5,7-dimethoxychromen-4-one 
• 132435-34-8 (R)-5,7-dimethoxy-3-(4-methoxybenzyl)chroman-4-one 
• 17934-14-4 (S)-5,7-dimethoxy-3-(4-methoxybenzyl)chroman-4-one 

Relevant articles and documents

Novel homoisoflavanone derivatives, preparation method thereof, and pharmaceutical composition for use in preventing or treating ischemic brain damage and multiple sclerosis containing the same as an active ingredient

The present invention relates to: a homoisoflavanone compound; a manufacturing method thereof; and a pharmaceutical composition for preventing or treating ischemic brain damage and multiple sclerosis containing the homoisoflavanone compound as an active i

Synthesis and NMR elucidation of homoisoflavanone analogues

A series of five homoisoflavanone analogues have been synthesized from the corresponding 3,5-methoxy phenols via chroman-4-one in three steps. The complete NMR elucidation of these homoisoflavanone analogues is reported. The use of 2D NMR techniques (COSY, NOESY, HSQC and HMBC) proved to be very useful tools in the elucidation of homoisoflavanone analogues. The homoisoflavanone analogues exhibit an AA0BB0 spin pattern in the ring B of the homoisoflavanone. These homoisoflavanone analogues are potential antifungal and anti-inflammatory agents. Springer Science+Business Media, LLC 2010.