6328-44-5

Usage

Uses

Used in Cosmetic and Personal Care Industry:
2-Propanoyloxybenzoic acid is used as a skin-conditioning agent for its ability to improve skin health and treat conditions such as acne and psoriasis.
Used in Pharmaceutical Industry:
2-Propanoyloxybenzoic acid is used as an analgesic and antipyretic agent in over-the-counter medications, providing relief from pain and fever.
However, it is important to note that 2-propanoyloxybenzoic acid should be used with caution due to its potential to cause skin irritation and allergic reactions in some individuals.

InChI:InChI=1/C10H10O4/c1-2-9(11)14-8-6-4-3-5-7(8)10(12)13/h3-6H,2H2,1H3,(H,12,13)

Upstream product

• 54-21-7 sodium salicylate 
• 79-03-8 propionyl chloride 
• 69-72-7 salicylic acid 
• 123-62-6 propionic acid anhydride 

Downstream Products

• 180421-55-0 2-Diethylcarbamoylphenyl Propionate 
• 315241-12-4 C₁₀H₁₀O₄C₆H₁₄Si 
• 13942-91-1 N-propionyl salicylamide 

Relevant academic research and scientific papers

Erbium(III) chloride: A very active acylation catalyst

Erbium(iii) chloride is a powerful catalyst for the acylation of alcohols and phenols. The reaction works well for a large variety of simple and functionalized substrates by using different kinds of acidic anhydrides (Ac 2O, (EtCO)2O, (PriCO)2O, (Bu tCO)2O, and (CF3CO)2), without isomerization of chiral centres. Moreover, the catalyst can be easily recycled and reused without significant loss of activity. CSIRO 2007.

A Novel Synthesis of 4H-Chromen-4-ones via Intramolecular Wittig Reaction

formula presented The acylphosphoranes formed in a sequential manner from the reaction of the silyl ester of O-acyl(aroyl)salicylic acids and (trimethylsilyl)-methylenetriphenylphosphorane undergo intramolecular Wittig cyclization on the ester carbonyl to afford the 4H-chromen-4-ones in good to excellent yields.

Modeling of controlled release of aspirin derivatives from human erythrocytes

The transport of aspirin (ASP) and its derivatives (m- or p-acetoxybenzoic acid (m- or p-AcOHBA), o-propionyloxybenzoic acid (PrOHBA), o-butyryloxybenzoic acid (BuOHBA), o-acetoxyhippuric acid (AcOHPA), and o-acetoxy-N-benzoyl-β-alanine (AcONBA)) through

Acylcobalt salophen complexes. Homolytic decomposition to salicyl aldehyde esters

Irradiation of acylcobalt salophen complexes leads to salicyl aldehyde ester products resulting from cobalt-to-oxygen migration.