795276-94-7

Upstream product

• 39895-55-1 4-(1,1-dimethylethyl)-benzenemethanamine 
• 1885-14-9 phenyl chloroformate 
• 622-46-8 carbamic acid phenyl ester 

Downstream Products

• 911143-54-9 N-{4-[3-(4-t-butylbenzyl)-ureidomethyl]-2-methylphenyl}-methanesulfonamide 
• 911124-83-9 1-(4-amino-3-fluoro-benzyl)-3-(4-t-butyl-benzyl)-urea 

Relevant academic research and scientific papers

PROCESS OF SULFONATING 4-AMINOBENZONITRILES

A process of producing a compound of formula (3), wherein R1 is a C1-5 alkyl group, R2 is a halogen atom, a C1-5 alkyl group, a C2-5 alkenyl group, a C2-5 alkynyl group, a C1-5 a

Reductive alkylation of thioureas: A highly practical synthesis of unsymmetrical N,N′-disubstituted thioureas

A highly practical synthesis of unsymmetrical N,N′-disubstituted thioureas by the reductive alkylation of N-monosubstituted thioureas with aldehydes is described. N-Monosubstituted thioureas can in turn be synthesized by the reductive amination of thiourea with an appropriate aldehyde. This reductive alkylation methodology was also extended to carbamates.