171973-40-3

Basic information

• Product Name: 2-hydroxy-4-(tetra-O-acetyl-β-D-glucopyranosyloxy)phenyl 4'-hydroxybenzyl ketone
• Synonyms: 2-hydroxy-4-(tetra-O-acetyl-β-D-glucopyranosyloxy)phenyl 4'-hydroxybenzyl ketone
• CAS NO: 171973-40-3
• Molecular Weight: 574.538
• Mol File: 171973-40-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-hydroxy-4-(tetra-O-acetyl-β-D-glucopyranosyloxy)phenyl 4'-hydroxybenzyl ketone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-hydroxy-4-(tetra-O-acetyl-β-D-glucopyranosyloxy)phenyl 4'-hydroxybenzyl ketone(171973-40-3)
• EPA Substance Registry System: 2-hydroxy-4-(tetra-O-acetyl-β-D-glucopyranosyloxy)phenyl 4'-hydroxybenzyl ketone(171973-40-3)

Safety Data

• Hazardous Substances Data: 171973-40-3(Hazardous Substances Data)

Upstream product

• 17720-60-4 2,4,4'-trihydroxy deoxybenzoin 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 

Downstream Products

• 552-66-9 daidzin 

Relevant articles and documents

SYNTHESIS OF 7-O-β-D-GLUCOPYRANOSIDES OF ISOFLAVONES AND THEIR HETEROCYCLIC ANALOGUES

The products of the interaction of α-acetobromoglucose with 2,4,5-trihydroxyphenyl benzyl ketone and 2,4-dihydroxyphenyl 4'-hydroxybenzyl ketone and also with their heterocyclic analogues, which are present completely or partially in the enolic form, have been investigated.It has been shown that in this reaction a tetra-O-acetylglucosyl residue is added at the 4-OH hydroxy group of the phenyl residue of the ketone.The compounds obtained have been converted into isoflavone 7-O-glucosides by the action of the Vilsmeier reagent or acetoformic anhydride.