55268-52-5

Usage

InChI:InChI=1/C13H8Cl4N2O/c14-7-1-3-11(9(16)5-7)18-13(20)19-12-4-2-8(15)6-10(12)17/h1-6H,(H2,18,19,20)

Upstream product

• 2612-57-9 2,4-dichlorophenyl isocyanate 
• 3893-00-3 N,N'-dichloro-N,N'-bis-(2,4-dichloro-phenyl)-urea 
• 554-00-7 2,4-Dichloroaniline 
• 57-13-6 urea 
• 7782-50-5 chlorine 
• 64-19-7 acetic acid 
• 197799-67-0 C₁₀H₁₂Cl₂N₂O 
• 88-10-8 N,N-diethylcarbamyl chloride 
• 89-75-8 2,4-dichlorobenzoyl chloride 

Downstream Products

• 3893-00-3 N,N'-dichloro-N,N'-bis-(2,4-dichloro-phenyl)-urea 
• 20632-35-3 bis(2,4,6-trichlorodiphenyl)urea 
• 2899-02-7 N,N'-dichlorobis(2,4,6-trichlorodiphenyl)urea 

Relevant academic research and scientific papers

Silicon-mediated direct conversion of acyl chlorides to carbamoyl azides or/and tetrazolinones under mild conditions

A simple and mild one-pot procedure for the synthesis of carbamoyl azides from acyl chlorides utilizing a combination of tetrachlorosilane and sodium azide in acetonitrile at ambient temperature is reported. Under gentle heating 1-aryltetrazolin-5- ones were also obtained in one-pot process presumably via a [3 + 2] cycloaddition step.

An unplanned synthesis of symmetrical 1,3-disubstituted ureas

When urea derivatives (N-aryl-N′, N'-dialkyl urea) or (N-aryl-N'-alkyl/arvl urea) la-lu react with diethylcarbamyl chloride at 50-60°C symmetrical 1,3-disubstituted ureas 2a-2f were furmed as major products instead of forming ployureas.