28520-50-5

Basic information

• Product Name: Benzoic acid, 2,4-bis(acetyloxy)-6-methyl-, ethyl ester
• CAS NO: 28520-50-5
• Molecular Formula: C14H16O6
• Molecular Weight: 280.277
• Mol File: 28520-50-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2,4-bis(acetyloxy)-6-methyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2,4-bis(acetyloxy)-6-methyl-, ethyl ester(28520-50-5)
• EPA Substance Registry System: Benzoic acid, 2,4-bis(acetyloxy)-6-methyl-, ethyl ester(28520-50-5)

Safety Data

• Hazardous Substances Data: 28520-50-5(Hazardous Substances Data)

Upstream product

• 2524-37-0 ethyl orselinate 
• 108-24-7 acetic anhydride 
• 67174-68-9 ethyl 4-hydroxy-2-oxo-6-methylcyclohex-3-ene-1-carboxylate 

Downstream Products

• 1071685-70-5 3,5-diacetyl-2,4-dihydroxy-6-methyl-benzoic acid 
• 17605-05-9 2-formyl-4,6-dimethoxy-benzoic acid ethyl ester 
• 28520-52-7 4,6-Dihydroxy-2-formyl-benzoesaeureethylester 
• 133156-40-8 (3,5-Diacetoxy-2-ethoxycarbonylbenzyl)triphenylphosphoniumbromid 
• 133156-42-0 2,4-Dihydroxy-3-(3-methyl-2-butenyl)-6-phenethylbenzoesaeuremethylester 
• 16929-92-3 2,4-dihydroxy-6-phenethylbenzoic acid methyl ester 
• 70610-12-7 2,4-Dihydroxy-3-(3-methyl-2-butenyl)-6-phenethylbenzoesaeure 
• 73436-04-1 2,4-Dihydroxy-3-geranyl-6-phenethylbenzoesaeure 
• 73436-05-2 2,4-Dihydroxy-3-geranyl-6-phenethylbenzoesaeuremethylester 
• 16964-24-2 (E/Z)-3,5-Dihydroxystilben-2-carbonsaeuremethylester 
• 4225-35-8 4,6-dimethoxycoumaranone 
• 133156-39-5 3,5-Diacetoxy-2-ethoxycarbonylbenzylbromid 
• 17605-04-8 2-(Diacetoxy-methyl)-4,6-diacetoxy-benzoesaeureethylester 

Relevant articles and documents

Synthesis of bryophyte components 2. Syntheses of prenylated bibenzyl derivatives

Efficient and expeditious syntheses of the biologically active prenylated bibenzyl derivatives 1a-d are developed giving rise to their access on a preparative scale.

Oxidation of Alkyl 1,6-Dihydroorsellinates. A New Method for the Synthesis of Methyl Orsellinate and Homologues

An efficient new procedure has been developed for the oxidation of the title compounds, utilizing one mole of bromine in the presence of acetic anhydride.