384837-22-3

Basic information

• Product Name: methyl 4-{[4-nitro-2-(trifluoromethyl)phenylimino]methyl}benzoate
• Synonyms: methyl 4-{[4-nitro-2-(trifluoromethyl)phenylimino]methyl}benzoate
• CAS NO: 384837-22-3
• Molecular Weight: 352.27
• Mol File: 384837-22-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 4-{[4-nitro-2-(trifluoromethyl)phenylimino]methyl}benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4-{[4-nitro-2-(trifluoromethyl)phenylimino]methyl}benzoate(384837-22-3)
• EPA Substance Registry System: methyl 4-{[4-nitro-2-(trifluoromethyl)phenylimino]methyl}benzoate(384837-22-3)

Safety Data

• Hazardous Substances Data: 384837-22-3(Hazardous Substances Data)

Upstream product

• 121-01-7 4-nitro-2-trifluoromethyl-aniline 
• 1571-08-0 methyl 4-formylbenzoate 

Downstream Products

• 1427066-93-0 methyl 4-{[4-nitro-2-(trifluoromethyl)phenylamino]methyl}benzoate 
• 1427066-98-5 methyl 4-[(4-amino-2-trifluoromethylphenylamino)methyl]benzoate 
• 364-13-6 2-(trifluoromethyl)-1,4-phenylenediamine 

Relevant articles and documents

Functionally substituted Schiff bases in reduction reactions

Functionally substituted Schiff bases obtained by the condensation of nitroaniline, pyrimidinylaminoaniline, 5-aminoquinoline, 5-aminoquinaldine derivatives with 4-methylformylbenzoate were studied in the reactions of sodium borohydride with acidic activators, hydrazine hydrate in the presence of Raney nickel, Raney alloy in the presence of potassium hydroxide. By the reduction of azomethines new benzyl derivatives of aniline, quinolylamine, arylaminopyrimidine, and phenylenediamine were obtained.