38501-85-8

Upstream product

• 89-95-2 2-methyl-benzyl alcohol 
• 108-42-9 3-chloro-aniline 
• 90-02-8 salicylaldehyde 

Downstream Products

• 881012-24-4 2-[1-[5-(3-Chloro-phenylazo)-2-hydroxy-phenyl]-meth-(E)-ylidene-hydrazinocarbonyl]-N-phenyl-acetamide 
• 881012-27-7 N-(4-Chloro-phenyl)-2-[1-[5-(3-chloro-phenylazo)-2-hydroxy-phenyl]-meth-(E)-ylidene-hydrazinocarbonyl]-acetamide 
• 881012-25-5 N-(2-Chloro-phenyl)-2-[1-[5-(3-chloro-phenylazo)-2-hydroxy-phenyl]-meth-(E)-ylidene-hydrazinocarbonyl]-acetamide 
• 881012-26-6 N-(3-Chloro-phenyl)-2-[1-[5-(3-chloro-phenylazo)-2-hydroxy-phenyl]-meth-(E)-ylidene-hydrazinocarbonyl]-acetamide 

Relevant academic research and scientific papers

Extending the scope of amantadine drug by incorporation of phenolic azo Schiff bases as potent selective inhibitors of carbonic anhydrase II, drug-likeness and binding analysis

A series of Amantadine-based azo Schiff base dyes 6a–6e have been synthesized and characterized by 1H NMR and 13C NMR and evaluated for their in vitro carbonic anhydrase II inhibition activity and antioxidant activity. All of the syn

Synthesis and antifungal screening of some new 1,3-diketo amino analogues

Few new 1,3-diketo amino compounds containing -NH-N = C linkage have been synthesized by incorporating chloro group at different positions and are reported along with their spectral data and antifungal properties.