882427-73-8

Basic information

• Product Name: 2,4-Bis-benzyloxy-6-(3,4-bis-benzyloxy-benzoyloxy)-benzoic acid benzyl ester
• Synonyms: 2,4-Bis-benzyloxy-6-(3,4-bis-benzyloxy-benzoyloxy)-benzoic acid benzyl ester
• CAS NO: 882427-73-8
• Molecular Weight: 756.852
• Mol File: 882427-73-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,4-Bis-benzyloxy-6-(3,4-bis-benzyloxy-benzoyloxy)-benzoic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-Bis-benzyloxy-6-(3,4-bis-benzyloxy-benzoyloxy)-benzoic acid benzyl ester(882427-73-8)
• EPA Substance Registry System: 2,4-Bis-benzyloxy-6-(3,4-bis-benzyloxy-benzoyloxy)-benzoic acid benzyl ester(882427-73-8)

Safety Data

• Hazardous Substances Data: 882427-73-8(Hazardous Substances Data)

Upstream product

• 83-30-7 acide 2,4,6-trihydroxybenzoique 
• 100-39-0 benzyl bromide 
• 99-50-3 3,4-Dihydroxybenzoic acid 
• 882427-72-7 3,4-(bisbenzyloxy)benzoic acid benzyl ester 
• 882427-70-5 benzyl 2,4-bis(benzyloxy)-6-hydroxybenzoate 
• 1570-05-4 3,4-bis(benzyloxy)benzoic acid 

Downstream Products

• 30048-34-1 2-(3',4'-dihydroxybenzoyloxy)-4,6-dihydroxybenzoic acid 

Relevant articles and documents

First chemical synthesis of three natural depsides involved in flavonol catabolism and related to quercetinase catalysis

We report here the first chemical synthesis of three depsides related to quercetinase-catalyzed degradation of kaempferol, quercetin, and myricetin. The three depsides were constructed through the coupling of suitably protected phloroglucinol carboxylic acid and hydroxy-perbenzylated, derivatives of gallic, protocatechuic, and 4-hydroxy benzoic acids. The three synthesized target compounds proved to be identical to their natural counterparts, arising from quercetinase action on corresponding flavonols. Copyright Taylor & Francis Group, LLC.