21524-25-4

Upstream product

• 106-48-9 4-chloro-phenol 
• 100-34-5 benzene diazonium chloride 
• 62-53-3 aniline 
• 2684-02-8 benzenediazonium 

Downstream Products

• 61-80-3 zoxazolamine 
• 22876-19-3 5-chlorobenzo[d]oxazole-2(3H)-thione 
• 332144-07-7 1-(5-chlorobenzo[d]oxazol-2-yl)guanidine 
• 95419-63-9 (ClC₆H₃(O)N₂C₆H₅)2Cu 
• 6237-59-8 hexamethyl benzenehexacarboxylate 
• 1710-10-7 tetramethyl furan-2,3,4,5-tetracarboxylate 
• 95-85-2 2-hydroxy-5-chloro-aniline 

Relevant academic research and scientific papers

Nanosilica/NaNO2: Novel heterogeneous system for synthesis of Azo compounds

Various azo compounds are synthesized by electrophonic substitution reaction in the presence of Nanosilica/NaNO2as a catalyst. Copyright Taylor & Francis Group, LLC.

Synthesis of some aryl azo-compounds under mild conditions

Some aryl azo compounds 2(a-h) were synthesized by reaction of corresponding aromatic amine and phenol derivatives under mild conditions. The yields of the products after recrysallization from acetic acid were in the order of 65-95 %. IR and 1H

Synthesis of diaryl-azo derivatives as potential antifungal agents

As compared with a commercially available agricultural fungicide hymexazol, some phenyl-azo phenol derivatives (e.g., 4a, 4b, 4f, 4n, 4q, 4u, and 4v) exhibited the more promising and pronounced antifungal activities in vitro against seven phytopathogenic fungi. It seemed that 4-((un)substituted phenylazo)-phenol and 4-((un)substituted phenylazo)-3-methylphenol might be considered as new lead structures for further design of agricultural fungicides.