970-31-0

Usage

Uses

Used in Plastics and Polymer Industry:
N,N-diphenylbenzohydrazide is used as a UV stabilizer for protecting plastics and polymers from the degrading effects of ultraviolet radiation. This application helps to extend the lifespan and maintain the quality of these materials.
Used in Pharmaceutical and Agrochemical Industries:
N,N-diphenylbenzohydrazide is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its role in these industries is crucial for the development of new and effective products.

Upstream product

• 18039-45-7 2,5-diphenyl-2H-tetrazole 
• 108-95-2 phenol 
• 98-88-4 benzoyl chloride 
• 530-50-7 1,1-Diphenylhydrazine 
• 532-96-7 N-benzoyl-N'-phenylhydrazine 
• 952-53-4 1,3-diphenyl-2,3-diazaprop-2-en-1-one 
• 106-44-5 p-cresol 
• 33491-26-8 Phenyl-N-phenyl-benzohydrazonat 
• 108-39-4 3-methyl-phenol 
• 95-48-7 ortho-cresol 
• 91-01-0 1,1-Diphenylmethanol 
• 952-53-4 (E)-phenyl(phenyldiazenyl)methanone 
• 1907-33-1 lithium tert-butoxide 
• 100-63-0 phenylhydrazine 

Downstream Products

• 724432-44-4 2,3-dibenzoyl-1,1,4,4-tetraphenyl-tetrazane 
• 65-85-0 benzoic acid 
• 530-50-7 1,1-Diphenylhydrazine 

Relevant academic research and scientific papers

Copper(ii)-catalyzed coupling reaction: An efficient and regioselective approach to N′,N′-diaryl acylhydrazines

Using N′-aryl acylhydrazines as aryl donors, a novel copper(ii)-catalyzed homo-coupling reaction of N′-aryl acylhydrazines has been developed for the synthesis of N′,N′-diaryl acylhydrazines. We also provided a complementary procedure for the preparation of unsymmetrical diaryl acylhydrazines via cross-coupling reaction. These protocols featured mild reaction conditions, wide functional group tolerance and highly regioselective products. Control experiments indicated that this kind of coupling reaction might undergo a transient acyl diazene intermediate. This journal is

KOt-Bu promoted homocoupling and decomposition of N'-aryl acylhydrazines: synthesis of unsymmetric N',N'-diaryl acylhydrazines

The KOt-Bu promoted homocoupling and decomposition of N'-aryl acylhydrazines has been achieved. The method allows for a novel and efficient synthesis of unsymmetric N',N'-diaryl acylhydrazines under mild reaction conditions. The reaction probably proceeds via the generation of N'-centered acylhydrazine radicals and the subsequent homolytic aromatic substitution.

An oxidative transformation of N′-phenylhydrazide to t-butyl ester using a copper(II) halide-lithium t-butoxide system

Reactions of hydrazides or N1-phenylhydrazides with a copper(II) reagent prepared from copper(II) bromide and lithium t-butoxide smoothly proceeded to give the corresponding t-butyl ester in high yield.

Reduction of Ag(I) by 1-acyl-2-arylhydrazines: Mechanism of photographic infectious development

The photographic process of 'infectious development' in which 1-acyl-2-arylhydrazines reduce Ag(I) has been studied using analogues. 1-Acyl-2-aryldiazenes, resulting from oxidation of 1-acyl-2-arylhydrazines, are hydrolysed to anions of aryldiazenes (ArN = NH), which undergo further oxidation with loss of nitrogen to yield aryl radicals. The aryl radicals cause 'feedback inhibition' which is prevented by the addition of benzhydrol.