2829-29-0

Usage

InChI:InChI=1/C14H13ClN2O/c1-18-14-8-2-11(3-9-14)10-16-17-13-6-4-12(15)5-7-13/h2-10,17H,1H3/b16-10+

Upstream product

• 932-98-9 1-chloro-4-nitroso-benzene 
• 2393-23-9 4-methoxy-benzylamine 
• 123-11-5 4-methoxy-benzaldehyde 
• 1073-69-4 N-4-chlorophenylhydrazine 

Downstream Products

• 113060-81-4 1,5-bis-(4-chloro-phenyl)-3-(4-methoxy-phenyl)-formazan 
• 1402441-44-4 1-(4-chlorophenyl)-3-(4-methoxyphenyl)-5-methyl-1H-pyrazole 
• 106737-54-6 6-chloro-3-(4-methoxy-phenyl)-benzo[e][1,2,4]triazine-1-oxide 
• 101094-87-5 6-chloro-3-(4-methoxy-phenyl)-benzo[e][1,2,4]triazine 

Relevant academic research and scientific papers

N-Aminations of Benzylamines and Alicyclic Amines with Nitrosoarenes to Hydrazones and Hydrazides

Unlike other alkylamines, benzylamines upon reaction with a nitrosoarene undergo oxidation to the corresponding imines. A direct amination of benzylamines, which was difficult to achieve due to its facile oxidation, to the corresponding hydrazones is reported. A wide variety of benzylamines and N-heterocycles were reacted with nitrosoarenes to provide structurally diverse hydrazones and hydrazides, respectively. Moreover, the direct N-amination reaction was applied to the one-pot synthesis of triazoles.

Synthesis, crystal structure, optical and electrochemical properties of novel diphenylether-based formazan derivatives

In this study, formazans 5a-5h were synthesized by coupling the reactions of substituted phenylhydrazone compounds 3a-3h with diazonium salt of 4-chloro-2-phenoxybenzenamine (4). The substituted phenylhydrazones 3a-3h were obtained from the condensation o