191164-60-0

Basic information

• Product Name: (3S,3aS,6S,6aR)-3-(3,4-Dihydroxy-benzyl)-3,3a,6-trihydroxy-tetrahydro-furo[3,2-b]furan-2-one
• Synonyms: (3S,3aS,6S,6aR)-3-(3,4-Dihydroxy-benzyl)-3,3a,6-trihydroxy-tetrahydro-furo[3,2-b]furan-2-one
• CAS NO: 191164-60-0
• Molecular Weight: 298.249
• Mol File: 191164-60-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3S,3aS,6S,6aR)-3-(3,4-Dihydroxy-benzyl)-3,3a,6-trihydroxy-tetrahydro-furo[3,2-b]furan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,3aS,6S,6aR)-3-(3,4-Dihydroxy-benzyl)-3,3a,6-trihydroxy-tetrahydro-furo[3,2-b]furan-2-one(191164-60-0)
• EPA Substance Registry System: (3S,3aS,6S,6aR)-3-(3,4-Dihydroxy-benzyl)-3,3a,6-trihydroxy-tetrahydro-furo[3,2-b]furan-2-one(191164-60-0)

Safety Data

• Hazardous Substances Data: 191164-60-0(Hazardous Substances Data)

Upstream product

• 139-85-5 3,4-dihydroxybenzaldehyde 
• 3897-89-0 4-(hydroxymethyl)benzene-1,2-diol 
• 50-81-7 ascorbic acid 

Relevant articles and documents

Reaction of vanilmandelic acid and 4-Hydroxybenzyl alcohol derivatives with L-ascorbic acid

The interaction between vanilmandelic and L-ascorbic acids led to a cyclopent-2-en-one derivative, whereas the reaction or methyl vanilmandelate with L-ascorbic acid yielded 2-furancarboxylic acid as the major product. The model 3-substituted 4-hydroxybenzyl alcohols and L-ascorbic acid produced ascorbigen-type structures, which easily decarboxylated to give mistures of the corresponding 1-aryl-1-deoxyketoses.