132017-98-2

Usage

Uses

Used in Pharmaceutical Formulations:
3-(2-HYDROXY-4-METHOXY-PHENYL)-3-OXO-PROPIONIC ACID METHYL ESTER is used as an antioxidant and anti-inflammatory agent in pharmaceutical formulations for its potential health benefits, including protection against oxidative damage and its anti-aging properties.
Used in Cosmetic Formulations:
In the cosmetic industry, 3-(2-HYDROXY-4-METHOXY-PHENYL)-3-OXO-PROPIONIC ACID METHYL ESTER is used as an active ingredient in skincare products for its antioxidant properties, which help protect the skin from environmental stressors and promote a youthful appearance.
Used in Skincare Products:
3-(2-HYDROXY-4-METHOXY-PHENYL)-3-OXO-PROPIONIC ACID METHYL ESTER is used as a key component in skincare products for its potential role in protecting cells from oxidative damage, promoting skin health, and contributing to anti-aging effects.
Used in Antioxidant Applications:
3-(2-HYDROXY-4-METHOXY-PHENYL)-3-OXO-PROPIONIC ACID METHYL ESTER is employed as a natural antioxidant in various applications, including food preservation and health supplements, due to its ability to neutralize free radicals and protect against oxidative stress.

Upstream product

• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 
• 616-38-6 carbonic acid dimethyl ester 

Downstream Products

• 396665-77-3 methyl 7-methoxy-2-(4-nitrobenzyl)-4H-1-benzopyran-4-one-3-carboxylate 
• 433682-93-0 methyl 7-methoxy-2-(4'-trifluoromethylbenzyl)-4H-1-benzopyran-4-one-3-carboxylate 
• 433682-95-2 7-methoxy-2-(4'-trifluoromethylbenzyl)-4H-1-benzopyran-4-one 
• 433682-94-1 7-methoxy-2-(4'-trifluoromethylbenzyl)-4H-1-benzopyran-4-one-3-carboxylic acid 
• 132018-28-1 2-(4-acetamidophenyl)-7-methoxy-3-(methoxycarbonyl)-4H-benzopyran-4-one 
• 132018-19-0 7-methoxy-2-(4-nitrophenyl)-4-oxo-4H-benzopyran-3-carboxylic acid 
• 132018-24-7 2-(4-hydroxyphenyl)-7-methoxy-3-(methoxycarbonyl)-4H-benzopyran-4-one 
• 132018-22-5 2-(4-hydroxyphenyl)-7-methoxy-4-oxo-4H-benzopyran-3-carboxylic acid 
• 131944-42-8 7-hydroxy-2-(4'-nitrophenyl)chromone 
• 132018-31-6 4'-amino-7-hydroxyflavone 
• 396665-78-4 7-methoxy-2-(4-nitrobenzyl)-4H-1-benzopyran-4-one-3-carboxylic acid 
• 396665-71-7 7-hydroxy-2-(4-nitro-benzyl)-chromen-4-one 
• 396665-79-5 7-methoxy-2-(4-nitrobenzyl)-4H-1-benzopyran-4-one 

Relevant academic research and scientific papers

Synthesis and Protein-Tyrosine Kinase Inhibitory Activities of Flavanoid Analogues

Treatment of o-hydroxyacetophenones 2a-e with excess lithium bis(trimethylsilyl)amide followed by dialkyl carbonates gave 3-(2-hydroxyaryl)-3-oxopropanoates 3a-e.The latter substances were transformed through the reaction of their magnesium chelates with