58822-01-8

Basic information

• Product Name: 2-(4-Benzyloxy-phenyl)-1-(2,4-bis-benzyloxy-phenyl)-3,3-dimethoxy-propan-1-one
• Synonyms: 2-(4-Benzyloxy-phenyl)-1-(2,4-bis-benzyloxy-phenyl)-3,3-dimethoxy-propan-1-one
• CAS NO: 58822-01-8
• Molecular Weight: 588.7
• Mol File: 58822-01-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(4-Benzyloxy-phenyl)-1-(2,4-bis-benzyloxy-phenyl)-3,3-dimethoxy-propan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-Benzyloxy-phenyl)-1-(2,4-bis-benzyloxy-phenyl)-3,3-dimethoxy-propan-1-one(58822-01-8)
• EPA Substance Registry System: 2-(4-Benzyloxy-phenyl)-1-(2,4-bis-benzyloxy-phenyl)-3,3-dimethoxy-propan-1-one(58822-01-8)

Safety Data

• Hazardous Substances Data: 58822-01-8(Hazardous Substances Data)

Upstream product

• 148356-55-2 2',4,4'-tris(benzyloxy)chalcone 
• 149-73-5 trimethyl orthoformate 
• 22877-01-6 2,4-bis(benzyloxy)acetophenone 
• 67-56-1 methanol 

Downstream Products

• 148356-33-6 daidzein 4',7-di-O-(tri-O-acetyl-α-L-rhamnopyranoside) 
• 148356-46-1 daidzein 4',7-di-O-(tri-O-acetyl-β-L-quinovopyranoside) 
• 148356-34-7 daidzein 4'-O-(tri-O-acetyl-α-L-rhamnopyranoside) 
• 148356-45-0 daidzein 7-O-(2,3,4-tri-O-acetyl-β-L-quinovopyranoside) 
• 4234-02-0 4',7-di-O-trimethylsilyloxyisoflavone 
• 486-66-8 daidzein 

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.