82448-61-1

Basic information

• Product Name: 2',4',5,7-tetrakis(benzyloxy)flavanone
• CAS NO: 82448-61-1
• Molecular Weight: 648.755
• Mol File: 82448-61-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2',4',5,7-tetrakis(benzyloxy)flavanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2',4',5,7-tetrakis(benzyloxy)flavanone(82448-61-1)
• EPA Substance Registry System: 2',4',5,7-tetrakis(benzyloxy)flavanone(82448-61-1)

Safety Data

• Hazardous Substances Data: 82448-61-1(Hazardous Substances Data)

Upstream product

• 100-44-7 benzyl chloride 
• 480-66-0 2,4,6-trihydroxyacetophenone 
• 13246-46-3 2,4-dibenzyloxybenzaldehyde 
• 18065-05-9 1-[2,4-bis(benzyloxy)-6-hydroxyphenyl]ethanone 

Downstream Products

• 96909-23-8 2',4',5,7-tetraacetoxy-3',5'-bis(3-methyl-2-butenyl)isoflavone 
• 96909-24-9 2',4',5,7-tetraacetoxy-5'-(3-methyl-2-butenyl)isoflavone 
• 96909-31-8 7-benzoyloxy-2',4',5-trihydroxy-3',5'-bis(3-methyl-2-butenyl)isoflavone 
• 96909-21-6 5-benzoyloxy-2',4',7-trihydroxy-3',5'-bis(3-methyl-2-butenyl)isoflavone 
• 96909-22-7 2',4',5,7-tetrahydroxy-3',5'-bis(3-methyl-2-butenyl)isoflavone 
• 82448-64-4 5-benzoyloxy-2',4',7-tris(benzyloxy)isoflavone 
• 82458-45-5 2',4',5,7-tetrakis(benzyloxy)isoflavone 
• 82448-63-3 2',4',7-tris(benzyloxy)-5-hydroxyisoflavone 
• 82448-70-2 7-benzoyloxy-2',4',5-trihydroxy-3'-(3-methyl-2-butenyl)isoflavone 
• 82448-66-6 5-benzoyloxy-2',4',7-trihydroxy-5'-(3-methyl-2-butenyl)isoflavone 
• 82448-71-3 7-benzoyloxy-2',4',5-trihydroxy-5'-(3-methyl-2-butenyl)isoflavone 
• 82448-69-9 7-benzoyloxy-2',4',5-trihydroxyisoflavone 
• 82448-65-5 5-benzoyloxy-2',4',7-trihydroxyisoflavone 
• 82448-67-7 2',4',5,7-tetrahydroxy-5'-(3-methyl-2-butenyl)isoflavone 

Relevant articles and documents

Synthesis of Licoisoflavone A and Related Compounds

2',4',5,7-Tetrahydroxyisoflavone was partially benzoylated with benzoyl chloride to give 7-benzoyloxy-2',4',5-trihydroxyisoflavone.The condensation of the 7-(benzoyloxy)isoflavone with 2-methyl-3-buten-2-ol, followed by the hydrolysis of the resultant 3'-(3-methyl-2-butenyl)isoflavone gave licoisoflavone A.Its 5'-(3-methyl-2-butenyl) isomer was also synthesized from 5-benzoyloxy-2',4',7-trihydroxyisoflavone in a similar manner.