17576-37-3

Upstream product

• 106-48-9 4-chloro-phenol 
• 104-12-1 p-chlorphenylisocyanate 
• 66285-88-9 3-(4-chloro-phenyl)-1-(1-cyano-cyclohexyl)-1-hydroxy-urea 
• 109-90-0 ethyl isocyanate 
• 64-17-5 ethanol 
• 66286-08-6 1-(4-chloro-phenylcarbamoyloxy)-N²-phenyl-3-oxa-1-aza-spiro[4.5]decane-2,4-diylidenediamine 

Downstream Products

• 856768-18-8 Ethyl-thiocarbamic acid O-(4-chloro-phenyl) ester 

Relevant academic research and scientific papers

Aminolysis of aryl N-ethyl thionocarbamates: Cooperative effects of atom pairs O and S on the reactivity and mechanism

The aminolysis reactions of aryl N-ethyl thionocarbamates (ETNC/EtHN-C(=S)-OC6H4Z) with benzylamines (XC 6H4CH2NH2) in acetonitrile are investigated at 30.0 °C. The rate of ETNC is slower b

Process for producing an aliphatic isocyanate

A process for producing an aliphatic isocyanate from an aliphatic primary amine comprising a carbonylation step in which an aliphatic primary amine is allowed to react with carbon monoxide at a temperature of about 100°-250° C. in the presence of an aromatic hydroxyl compound having a pKa value of not more than about 11, molecular oxygen and a catalyst system comprising at least one member selected from palladium and rhodium metals and components thereof and at least one member selected from iodine and bromine and compounds thereof and a combined separation and recovery step comprising a pyrolysis-distillation reaction in which the mixture of carbonylated products is heated to a temperature of from about 100° to 300° C.