3954-13-0

Usage

Uses

Used in Automotive Industry:
Pentyl isocyanate is used as a key component in car paint formulations, specifically for 1,6-hexamethylenediisocyanate-based (HDI) car paints. Its incorporation into the paint enhances the durability, gloss, and overall appearance of the automotive finish, making it a valuable addition to the automotive industry.
Used in Research and Development:
Pentyl isocyanate also serves as a useful research chemical for proteomic research. Its unique chemical properties allow scientists to study protein interactions and develop new methods for protein analysis, contributing to the advancement of scientific knowledge in the field of proteomics.

InChI:InChI=1/C6H11NO/c1-2-3-4-5-7-6-8/h2-5H2,1H3

Upstream product

• 112343-33-6 pentamethylene-1,5-di(methyl carbamate) 
• 128-09-6 N-chloro-succinimide 

Downstream Products

• 91904-97-1 1-(4-methoxyphenyl)-3-pentylurea 
• 93137-17-8 N-(3-nitro-phenyl)-N'-pentyl-urea 
• 74296-48-3 2,3-dihydro-5-(3',4'-dichlorophenyl)-6,7-bis(hydroxymethyl)-1H-pyrrolizine bis(pentylcarbamate) 
• 104017-75-6 C₁₄H₁₇F₆N₃O 
• 1026693-18-4 1-(2-Fluoro-6-methoxy-phenyl)-3-pentyl-urea 
• 1027526-40-4 1-(2-Chloro-6-methoxy-phenyl)-3-pentyl-urea 
• 1027924-09-9 1-(2-Ethyl-6-methoxy-phenyl)-3-pentyl-urea 
• 1026380-38-0 1-(2-Isopropyl-6-methoxy-phenyl)-3-pentyl-urea 
• 1026529-09-8 1-(2-Methoxy-6-propyl-phenyl)-3-pentyl-urea 
• 1026065-48-4 1-(2-Cyano-6-methoxy-phenyl)-3-pentyl-urea 
• 1027578-47-7 1-(2-Methoxy-6-methylsulfanyl-phenyl)-3-pentyl-urea 
• 1026879-61-7 1-(2-Hydroxymethyl-6-methoxy-phenyl)-3-pentyl-urea 
• 1026639-34-8 1-(2-Dimethylaminomethyl-6-methoxy-phenyl)-3-pentyl-urea 
• 149156-19-4 1-(6-Dimethylamino-2-methoxy-3-methyl-phenyl)-3-pentyl-urea 

Relevant academic research and scientific papers

Method for manufacturing pentamethylene diisocyanate

The present invention provides a method for manufacturing pentamethylene diisocyanate. The method for manufacturing pentamethylene diisocyanate of the present invention manufactures intermediates by using dialkyl carbonate. By thermally decomposing the intermediates under a specific polymerization inhibitor, the method can manufacture the pentamethylene diisocyanate having excellent purity in a high yield.

Synthesis and solid state and solution characterization of mono- and di-(η1-C) carbamoyl-palladium complexes. New efficient palladium-catalyzed routes to carbamoyl chlorides: Key intermediates to isocyanates, carbamic esters, and ureas

The catalytic conversion of primary and secondary amines into isocyanates or carbamoyl chlorides is performed using palladium complexes. The palladium-based catalytic systems is very active and avoids the synthesis of phosgene. The palladium (II) complex

Heterocyclic compounds having MMP and TNF inhibitory activity

Compounds of formula (I) are useful as therapeutic agents, by virtue of having MMP and TNF inhibitory activity.