15116-14-0

Usage

General Description

1-Butanone, 1-(2,4-dihydroxyphenyl)-3-methyl- is a chemical compound that is also known as 1-(2,4-dihydroxyphenyl)-3-methyl-2-butanone or 3-Methyl-1-(2,4-dihydroxyphenyl)-2-butanone. It is a derivative of butanone, which is a colorless liquid with a sweet, pungent odor. 1-Butanone, 1-(2,4-dihydroxyphenyl)-3-methyl- is commonly used in the production of various fragrances and flavors. It is also used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Additionally, it has potential applications in the field of medicine and can be used as an ingredient in some cosmetic products. However, it should be handled with care due to its potential health hazards, including skin and eye irritation and harmful effects if ingested or inhaled.

Upstream product

• 108-12-3 isopentanoyl chloride 
• 108-46-3 recorcinol 
• 503-74-2 3-methylbutyric acid 
• 625-28-5 Isovaleronitrile 
• 109043-63-2 2,4-dihydroxy-5-(3-methyl-crotonoyl)-benzoic acid methyl ester 
• 97025-37-1 2,4-dihydroxy-5-isovaleryl-benzoic acid methyl ester 
• 2150-47-2 methyl 2,4-dihydroxybenzoate 
• 3350-78-5 3,3-Dimethylacryloyl chloride 
• 92958-68-4 2,4-dihydroxy-5-isovaleryl-benzoic acid 

Downstream Products

• 251463-54-4 2,4-diacetoxyphenyl isobutyl ketone 
• 1204737-61-0 1-(2,4-dihydroxy-3-iodo-phenyl)-3-methyl-butan-1-one 
• 15116-20-8 2-Methoxy-5-(3-methyl-butyl)-p-benzochinon-(1,4) 
• 193687-88-6 1-(2-hydroxy-4-methoxyphenyl)-3-methylbutan-1-one 
• 15116-17-3 4-isopentyl-resorcinol 

Relevant academic research and scientific papers

IMIDAZOLE CARBOXAMIDES

The present invention provides certain imidazole carboxamide derivatives, pharmaceutical compositions thereof, methods of using the same and processes for preparing the same.

Synthesis and lipase-mediated stereoselective deacetylation of (±)-3-acetoxymethyl-3-alkyl-7-methoxychroman-4-ones

Six (±)-3-acetoxymethyl-3-alkyl-7-methoxychroman-4-ones have been synthesized in four steps starting with the coupling of resorcinol with corresponding aliphatic acid leading to the formation of 2,4-dihydroxyphenyl alkyl ketones, which upon monomethylation and hydroxymethylation, followed by acetylation afforded the racemic acetoxymethylated compounds in 17-30% overall yields. Candida rugosa lipase-catalyzed deacetylation of (±)-3-acetoxymethylchromanones in diisopropyl ether exhibited fairly moderate enantioselectivity.

Polyhydroxyphenol derivatives and preventive and therapeutic agents for bone and cartilage diseases containing the same

Compounds useful as preventive and therapeutic agents for bone and cartilage diseases; and drug compositions containing the same. The compounds are polyhydroxyphenol derivatives of general formula (I) and quinione analogues derived therefrom (wherein Rsu

Lipase-catalysed regio- and enantioselective deacetylation of 2,4-diacetoxyphenyl alkyl ketones

Porcine pancreatic lipase in tetrahydrofuran catalyses the deacetylation of 2,4-diacetoxyphenyl alkyl ketones in a highly regioselective fashion. The strategy of regioselective deacetylation of diacetoxyphenyl alkyl ketones has also resulted in the enanti