160154-75-6

Basic information

• Product Name: 2',4',5,7-tetrakis(benzoyloxy)-8-(3-hydroxy-3-methylbutyl)isoflavone
• Synonyms: 2',4',5,7-tetrakis(benzoyloxy)-8-(3-hydroxy-3-methylbutyl)isoflavone
• CAS NO: 160154-75-6
• Molecular Weight: 788.807
• Mol File: 160154-75-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2',4',5,7-tetrakis(benzoyloxy)-8-(3-hydroxy-3-methylbutyl)isoflavone(CAS DataBase Reference)
• NIST Chemistry Reference: 2',4',5,7-tetrakis(benzoyloxy)-8-(3-hydroxy-3-methylbutyl)isoflavone(160154-75-6)
• EPA Substance Registry System: 2',4',5,7-tetrakis(benzoyloxy)-8-(3-hydroxy-3-methylbutyl)isoflavone(160154-75-6)

Safety Data

• Hazardous Substances Data: 160154-75-6(Hazardous Substances Data)

Upstream product

• 160154-71-2 2'-acetoxy-2,4,4',6'-tetrakis(benzyloxy)-3'-iodochalcone 
• 160154-72-3 1-<2-acetoxy-4,6-bis(benzyloxy)-3-iodophenyl>-2-<2,4-bis(benzyloxy)phenyl>-3,3-dimethoxypropan-1-one 
• 160154-74-5 2',4',5,7-tetrakis(benzyloxy)-8-(3-hydroxy-3-methyl-1-butynyl)isoflavone 
• 160154-73-4 2',4',5,7-tetrakis(benzyloxy)-8-iodoisoflavone 
• 115-19-5 2-methyl-but-3-yn-2-ol 
• 98-88-4 benzoyl chloride 
• 104691-93-2 2',4',5,7-tetrahydroxy-8-(3-hydroxy-3-methylbutyl)isoflavone 

Downstream Products

• 74161-25-4 5,7,2',4'-tetrahydroxy-8-(3,3-dimethylallyl)isoflavone 
• 160154-76-7 2',4',5,7-tetrakis(benzoyloxy)-8-(3-methyl-2-butenyl)isoflavone 

Relevant articles and documents

Regioselective synthesis of prenylisoflavones. Syntheses of allolicoisoflavone A, 2,3-dehydrokievitone, and related compounds

The palladium-catalyzed coupling reaction of 2',4',5,7- tetrakis(benzyloxy)-5'-iodolsoflavone (12), synthesized from the 5- iodochalcone 9, with 2-methyl-3-butyn-2-ol gave the corresponding 5'-(3- hydroxy-3-methyl-1-butynyl)isoflavone 13. The catalytic hydrogenation of 13 gave 2',4',5,7-tetrahydroxy-5'-(3-hydroxy-3-methylbutyl)isoflavone (2). Dehydration of the benzoate 14 of 2 afforded a mixture of 5'-(3-methyl-2- butenyl)isoflavone 15 and the isomer 5'-(3-methyl-3-butenyl)isoflavone 16. The separation of 15 was accomplished by a treatment of the mixture (15 and 16) with mercury(II) nitrate. Hydrolysis of 15 afforded 2',4',5,7- tetrahydroxy-5'-prenylisoflavone (allolicoisoflavone A) (1). In a similar manner, 2',4',5,7-tetrahydroxy-8-prenylisoflavone (2,3-dehydrokievitone) (3) and 2',4',5,7-tetrahydroxy-8-(3-hydroxy-3-methylbutyl)isoflavone (2,3- dehydrokievitone hydrate) (4) were synthesized from the corresponding 8- iodoisoflavone 22. The tetramethyl ether 5 of 3 was also prepared from the 8- iodotetramethoxyisoflavone 32.