848653-50-9

Basic information

• Product Name: 5-(3-acetoxy-4-methoxy-phenyl)-4-hydroxy-pentanoic acid methyl ester
• Synonyms: 5-(3-acetoxy-4-methoxy-phenyl)-4-hydroxy-pentanoic acid methyl ester
• CAS NO: 848653-50-9
• Molecular Weight: 296.32
• Mol File: 848653-50-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-(3-acetoxy-4-methoxy-phenyl)-4-hydroxy-pentanoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(3-acetoxy-4-methoxy-phenyl)-4-hydroxy-pentanoic acid methyl ester(848653-50-9)
• EPA Substance Registry System: 5-(3-acetoxy-4-methoxy-phenyl)-4-hydroxy-pentanoic acid methyl ester(848653-50-9)

Safety Data

• Hazardous Substances Data: 848653-50-9(Hazardous Substances Data)

Upstream product

• 90-05-1 2-methoxy-phenol 
• 613-70-7 2-methoxyphenyl acetate 
• 39716-58-0 pent-4-enoyl chloride 
• 591-80-0 pent-4-enoic acid 
• 818-57-5 Methyl 4-pentenoate 
• 183593-98-8 5-iodo-2-methoxyphenyl acetate 

Downstream Products

• 848653-51-0 5-(3-hydroxy-4-methoxy-benzyl)-dihydro-furan-2-one 
• 72719-14-3 5-(3,4-dimethoxybenzyl)dihydrofuran-2(3H)-one 
• 21618-92-8 5-(3′,4′-dihydroxyphenyl)-γ-valerolactone 
• 848653-56-5 4-hydroxy-5-(3-hydroxy-4-methoxy-phenyl)-pentanoic acid 

Relevant articles and documents

Synthesis and biological activity of the tea catechin metabolites, M4 and M6 and their methoxy-derivatives

Syntheses are reported for metabolites M4 (1) and M6 (2) of the green tea polyphenols epicatechin (EC) and epigallocatechin (EGC) and their gallate derivatives. Several methoxy-derivatives of 1 and 2 were also prepared. Compounds 1 and 2 were evaluated for growth inhibitory activity against a panel of immortalized and malignant human cell lines with 1 being the more active compound. The possible antiinflammatory activity of 1 and its trimethoxy derivative was also evaluated. Neither compound inhibited the release of arachidonic acid, although 1 inhibited NO production by 50% at 20 μM.