1437307-75-9

Basic information

• Product Name: 5-benzoyl-4'-hydroxy-6-C-(2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranosyl)-7-methoxyflavone
• Synonyms: 5-benzoyl-4'-hydroxy-6-C-(2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranosyl)-7-methoxyflavone
• CAS NO: 1437307-75-9
• Molecular Weight: 718.668
• Mol File: 1437307-75-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-benzoyl-4'-hydroxy-6-C-(2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranosyl)-7-methoxyflavone(CAS DataBase Reference)
• NIST Chemistry Reference: 5-benzoyl-4'-hydroxy-6-C-(2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranosyl)-7-methoxyflavone(1437307-75-9)
• EPA Substance Registry System: 5-benzoyl-4'-hydroxy-6-C-(2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranosyl)-7-methoxyflavone(1437307-75-9)

Safety Data

• Hazardous Substances Data: 1437307-75-9(Hazardous Substances Data)

Upstream product

• 74808-09-6 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate 
• 89025-46-7 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl fluoride 
• 169566-44-3 6-benzyloxy-3-C-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-2-hydroxy-4-methoxyacetophenone 
• 10299-59-9 1‐(2‐(benzyloxy)‐6‐hydroxy‐4‐methoxyphenyl)ethan‐1‐one 
• 1437307-74-8 4'-acetoxy-5-benzoyl-6-C-(2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranosyl)-7-methoxyflavone 
• 1437307-71-5 5-benzoyl-4'-benzyloxy-6-C-(2'',3'',4'',6''-tetra-O-benzyl-β-D-glucopyranosyl)-7-methoxyflavone 

Downstream Products

• 1437307-76-0 5-benzoyl-6-C-(2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranosyl)-4'-O-(2''',3''',4''',6'''-tetra-O-acetyl-β-D-glucopyranosyl)-7-methoxyflavone 
• 16049-42-6 Flavocommelin 

Relevant articles and documents

Concise synthesis of flavocommelin, 7-O-methylapigenin 6-C-, 4′-O-bis-β-d-glucoside, a component of the blue supramolecular pigment from Commelina communis

Flavocommelin, 7-O-methylapigenin 6-C-, 4′-O-bis-β-d-glucoside, was synthesized in 9 steps from the C-glycosylation of 6-O-benzy-4-O- methylphloroacetophenone via the introduction of a cinnamoyl residue by aldol condensation and the formation of a C-ring by regioselective and oxidative ring-closure to regio- and stereoselective O-glycosylation for an overall yield of 31%.