2998-08-5

Usage

Uses

Used in Polymer and Resin Production:
SEC-BUTYL ACRYLATE is used as a monomer for the production of various polymers and resins, contributing to their formation and properties.
Used in Adhesives Synthesis:
In the adhesives industry, SEC-BUTYL ACRYLATE is used as a raw material in the synthesis of adhesives, enhancing their bonding and adhesive properties.
Used in Coatings Production:
SEC-BUTYL ACRYLATE is utilized as a component in the production of coatings, improving their durability, adhesion, and other performance characteristics.
Used in Sealants Synthesis:
In the sealants industry, SEC-BUTYL ACRYLATE is used as a raw material in the synthesis of sealants, providing them with enhanced sealing and bonding capabilities.

InChI:InChI=1/C7H12O2/c1-4-6(3)9-7(8)5-2/h5-6H,2,4H2,1,3H3

Upstream product

• 292638-85-8 acrylic acid methyl ester 
• 78-92-2 iso-butanol 
• 79-10-7 acrylic acid 
• 814-68-6 acryloyl chloride 
• 57-57-8 β-Propiolactone 
• 78-76-2 s-butyl bromide 
• 74-86-2 acetylene 

Downstream Products

• 79-10-7 acrylic acid 
• 1121-05-7 2,3-dimethylcyclopent-2-enone 
• 132876-34-7 1-(2-sec-Butoxycarbonyl-ethyl)-4-(phenyl-propionyl-amino)-piperidine-4-carboxylic acid methyl ester 
• 112032-51-6 3-sec-butoxy-propionic acid sec-butyl ester 

Relevant academic research and scientific papers

Diastereomeric excess upon cleavage and reformation of diastereomeric alkoxyamines

The thermal reactions of several TEMPO and DEPN (N-(2-methylpropan-2-y1)-N-(1-diethylphosphono-2,2-dimethylpropyl)-aminoxyl) based alkoxyamines were studied by means of 1H and 31P NMR spectroscopy aiming to distinguish the contributions of diastereoselective homolysis and coupling to the total equilibrium diastereomeric distribution. The TEMPO-based compounds reveal no diastereomeric excess while DEPN based compounds show a moderate excess both upon homolysis and coupling. The diastereomeric preference of homolysis for DEPN-(propionate-like) adducts does not depend on the ester group and it is mainly affected by the size of β-substituents. The diastereoselective coupling is sensitive to the total recombination rate constant kc and diastereoselectivity increases with the decrease of kc. Small diastereoselective coupling is found in the recombination of DEPN with sec-butyl isobutyrate radical, where no prochiral centers are formed upon cleavage of corresponding alkoxyamine.

Novel antibacterial agents and potentiators of carbapenem antibiotics

New 3-(1-aminoalkylphosphinyl)-(2-substituted)propionic acids are described which display antibacterial activity and potentiate carbapenem antibiotics.