69732-95-2

Upstream product

• 455-14-1 4-trifluoromethylphenylamine 

Downstream Products

• 937279-35-1 tert-butyl 2-(4-(trifluoromethyl)phenyl)hydrazine-1-carboxylate 
• 1338369-60-0 N-tert-butoxycarbonyl-N'-(4-trifluoromethylphenyl)diazene 
• 1338369-66-6 N-tert-butoxycarbonyl-N'-(4-trifluoromethylphenyl)-N'-(3-chlorophenyl)hydrazine 
• 1338369-68-8 N-tert-butoxycarbonyl-N'-(4-trifluoromethylphenyl)-N'-phenylhydrazine 
• 1338369-69-9 N-tert-butoxycarbonyl-N'-(2-methoxyphenyl)-N'-(4-trifluoromethylphenyl)hydrazine 
• 1338369-79-1 N'-(4-trifluoromethylphenyl)-N'-(3-chlorophenyl)hydrazine 
• 1338369-75-7 N-(3-chlorophenyl)-4-trifluoromethylaniline 
• 1338369-76-8 N-(2-methoxyphenyl)-N-(4-trifluoromethyl)aniline 
• 53451-87-9 phenyl(4-trifluoromethylphenyl)amine 
• 368-90-1 4-(trifluoromethyl)phenylhydrazine 

Relevant academic research and scientific papers

Photoinduced cleavage of N-N bonds of aromatic hydrazines and hydrazides by visible light

A photocatalytic system involving [Ru(bpyrz)(PFH, visible light, and air has been developed for cleavage of the N-N bonds of hydrazines and hydrazides. This catalytic system is generally effective for N,N-disubstituted hydrazine and hydrazide derivatives, including arylhydrazides, N-alkyl-N-arylhydrazines, and N,N-diarylhydrazines. The utility of this cleavage reaction has been demonstrated by synthesizing a variety of secondary aromatic amines. Georg Thieme Verlag Stuttgart ? New York.

Fungicidal phenylnitramines and new phenylnitramines

The present invention relates to novel methods for the protection of agricultural crops against plant pathogenic fungi comprising applying to the foliage of said crops a fungicidally effective amount of a compound selected from certain substituted phenylnitramines and certain novel salts of 2,3,5,6-tetrachlorophenylnitramine. The present invention further relates to certain novel substituted phenylnitramine and certain novel salts of 2,3,5,6-tetrachlorophenylnitramine and methods of preparation thereof.