118364-66-2

Upstream product

• 1013-88-3 Benzophenone imine 
• 118364-52-6 1-phenyl-1--2,2,2-trifluoroethyl 4-bromobenzoate 
• 64-17-5 ethanol 
• 107-56-2 O,O-diisopropyl hydrogen phosphorodithioate 
• 108-95-2 phenol 
• 65-85-0 benzoic acid 
• 118364-56-0 1-(4-Bromo-benzoyl)-3-[2,2,2-trifluoro-1-phenyl-eth-(Z)-ylidene]-1-(2,4,6-trimethyl-phenyl)-urea 
• 106-54-7 p-Chlorothiophenol 
• 298-06-6 O,O-Diethyl hydrogen phosphorodithioate 
• 64-19-7 acetic acid 
• 120-80-9 benzene-1,2-diol 
• 2563-26-0 4,5-dibromobenzene-1,2-diol 
• 126681-29-6 1-(4-Bromo-benzoyl)-3-[2,2,2-trifluoro-1-p-tolyl-eth-(Z)-ylidene]-1-(2,4,6-trimethyl-phenyl)-urea 
• 3428-24-8 4,5-dichlorocatechol 

Downstream Products

• 118364-56-0 1-(4-Bromo-benzoyl)-3-[2,2,2-trifluoro-1-phenyl-eth-(Z)-ylidene]-1-(2,4,6-trimethyl-phenyl)-urea 
• 126681-29-6 1-(4-Bromo-benzoyl)-3-[2,2,2-trifluoro-1-p-tolyl-eth-(Z)-ylidene]-1-(2,4,6-trimethyl-phenyl)-urea 

Relevant academic research and scientific papers

N-CARBODIIMIDES. II. REACTIONS WITH CARBOXYLIC ACIDS AND O,O-DIALKYL HYDROGEN DITHIOPHOSPHATES

The reaction of N-carbodiimides with carboxylic acids and O,O-dialkyl hydrogen dithiophosphates is accompanied by fragmentation of the carbodiimide molecule and leads to the formation of N-substituted amides and 1-(acyloxy)alkyl isocyana

N-CARBODIIMIDES. ISOMERIC TRANSFORMATIONS AND REACTIONS WITH PROTON-CONTAINING NUCLEOPHILIC REAGENTS

The conditions for the isomerization of N-carbodiimides to N-alkylidene-N'-acylureas were investigated.In the reaction of N-carbodiimides with alcohols, phenols, thiophenols, and imines fragmentation of the carbodiimides occurs with the formation of 1-alkoxy-, 1-aryloxy-, 1-arylthio-, and 1-alkylideneaminoalkyl isocyanates and amides.The products from the reaction with water and with tert-butylamine are the amide, ketone, and N-alkylimine.