126495-72-5

Basic information

• Product Name: methyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate
• Synonyms: methyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate
• CAS NO: 126495-72-5
• Molecular Weight: 224.213
• Mol File: 126495-72-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: methyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate(126495-72-5)
• EPA Substance Registry System: methyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate(126495-72-5)

Safety Data

• Hazardous Substances Data: 126495-72-5(Hazardous Substances Data)

Upstream product

• 819812-55-0 methyl 2-acetyl-3,5-diallyloxyphenylacetate 
• 916197-35-8 C₇H₈O₃ 
• 74590-73-1 1,3-bis(trimethylsiloxy)-1-methoxybuta-1,3-diene 
• 4724-10-1 methyl 2-(3,5-dihydroxyphenyl)acetate 
• 108-24-7 acetic anhydride 
• 65857-78-5 methyl 2-acetyl-3,5-bis(benzyloxy)phenylacetate 
• 6512-33-0 2-acetyl-3,5-dimethoxyphenylacetic acid methyl ester 
• 58604-84-5 (3',5'-dibenzyloxy)phenylacetonitrile 
• 2732-96-9 3,5-dibenzyloxyphenylacetic acid 
• 58605-10-0 methyl 3,5-bis(benzyloxy)benzoate 
• 79762-35-9 methyl 2-(3,5-bis(benzyloxy)-2-formylphenyl)acetate 
• 24131-31-5 3,5-dibenzyloxybenzyl alcohol 

Downstream Products

• 479-05-0 flaviolin 
• 49598-85-8 3,6,8-Trihydroxy-3,4-dihydronaphthalen-1(2H)-one 
• 77053-29-3 6,8-dihydroxy-1-methylisochroman-3-one 
• 1389342-19-1 C₁₇H₁₄O₇ 
• 1389342-17-9 C₁₇H₁₄O₇ 
• 1389342-53-3 C₂₉H₂₈O₁₁ 
• 1389342-32-8 C₁₈H₁₅ClO₆ 
• 1389341-60-9 C₂₃H₃₂O₇ 
• 1389342-26-0 C₁₉H₁₈O₇ 
• 1389342-23-7 C₁₈H₁₆O₇ 
• 1389342-27-1 C₁₈H₁₆O₆ 

Relevant articles and documents

A unifying paradigm for naphthoquinone-based meroterpenoid (bio)synthesis

Bacterial meroterpenoids constitute an important class of natural products with diverse biological properties and therapeutic potential. The biosynthetic logic for their production is unknown and defies explanation via classical biochemical paradigms. A l

A total synthesis of xestodecalactone A and proof of its absolute stereochemistry: Interesting observations on dienophilic control with 1,3-disubstituted nonequivalent allenes

A concise total synthesis of xestodecalactone A, utilizing a Diels-Alder strategy is described. The focal Diels-Alder reaction relied on an "ynoate" dienophile to rapidly assemble the required resorcylinic acid scaffold. During this study, Diels-Alder cycloaddition reactions involving 1,3-disubstituted nonequivalent allene dienophiles were studied, and some surprising results were encountered.

DEOXYGENATION IN THE BIOSYNTHESIS OF POLYKETIDES: MECHANISM OF BIOMIMETIC REDUCTION OF TETRAHYDROXYNAPHTHALENE

A biomimetic synthesis of scytalone, a simple derivative of tetralone, was reinvestigeted using NMR spectroscopy.Scytalone was formed from 1,3,6,8-tetrahydroxynaphthalene (1,3,6,8-THN) by sodium borohydride reduction only in the presence of sodium methoxi