882427-70-5

Basic information

• Product Name: benzyl 2,4-bis(benzyloxy)-6-hydroxybenzoate
• Synonyms: benzyl 2,4-bis(benzyloxy)-6-hydroxybenzoate
• CAS NO: 882427-70-5
• Molecular Weight: 440.496
• Mol File: 882427-70-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl 2,4-bis(benzyloxy)-6-hydroxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 2,4-bis(benzyloxy)-6-hydroxybenzoate(882427-70-5)
• EPA Substance Registry System: benzyl 2,4-bis(benzyloxy)-6-hydroxybenzoate(882427-70-5)

Safety Data

• Hazardous Substances Data: 882427-70-5(Hazardous Substances Data)

Upstream product

• 882427-71-6 5,7-bis(benzyloxy)-2,2-dimethyl-4H-1,3-benzodioxin-4-one 
• 20194-18-7 sodium phenyl-methanolate 
• 83-30-7 acide 2,4,6-trihydroxybenzoique 
• 100-39-0 benzyl bromide 

Downstream Products

• 1243583-64-3 benzyl 2,4-bis(benzyloxy)-6-(((trifluoromethyl)sulfonyl)-oxy) benzoate 
• 30048-34-1 2-(3',4'-dihydroxybenzoyloxy)-4,6-dihydroxybenzoic acid 
• 882427-75-0 C₅₆H₄₆O₉ 
• 882427-73-8 2,4-Bis-benzyloxy-6-(3,4-bis-benzyloxy-benzoyloxy)-benzoic acid benzyl ester 

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.