4996-43-4

Basic information

• Product Name: 2',4-bis(benzyloxy)chalcone
• Synonyms: 2',4-bis(benzyloxy)chalcone
• CAS NO: 4996-43-4
• Molecular Weight: 420.508
• Mol File: 4996-43-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2',4-bis(benzyloxy)chalcone(CAS DataBase Reference)
• NIST Chemistry Reference: 2',4-bis(benzyloxy)chalcone(4996-43-4)
• EPA Substance Registry System: 2',4-bis(benzyloxy)chalcone(4996-43-4)

Safety Data

• Hazardous Substances Data: 4996-43-4(Hazardous Substances Data)

Upstream product

• 4397-53-9 p-benzyloxybenzaldehyde 
• 31165-67-0 2'-benzyloxyacetophenone 

Downstream Products

• 148356-67-6 4'-hydroxyisoflavone (tri-O-acetyl-α-L-rhamnopyranoside) 
• 58113-14-7 3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 

Relevant articles and documents

Syntheses of Isoflavones and Isoflavone Glycosides, and Their Inhibitory Activity against Bovine Liver &β-Galactosidase

To clarify the relationship between the structure and inhibitory action toward β-D-galactosidase (EC 3.2.1.21) of isoflavones and isoflavone glycosides, a number of polyhydroxyisoflavones, and the α-L-rhamnosides and β-L-quinovosides of daidzein and genistein were synthesized.Among the polyhydroxyisoflavones, 2',3',4',7-tetrahydroxyisoflavone showed the strongest inhibitory activity (Ki = 26 * 10-6 M).Among the glycosides, all the L-rhamnosides were strong inhibitors, of which genistein 4',7-di-O-α-L-rhamnoside was the strongest (Ki = 4.44 * 10-6 M), while all the isoflavone β-L-quinovosides were considerably weak or possessed no inhibition.