82485-86-7

Usage

Structure

1H-Tetrazole derivative with 1-phenyland 5-(2,6-dimethylphenoxy) substitution

Usage

Synthesis of pharmaceuticals, agrochemicals, and dyes

Biological and pharmacological activities

Potential anti-cancer agent, ability to inhibit the growth of certain strains of bacteria

Versatility

A versatile building block for the creation of diverse compounds

Ongoing research and development

Uses continue to be explored in various fields of research and development.

Upstream product

• 14210-25-4 5-Chloro-1-phenyltetrazole 
• 576-26-1 2.6-dimethylphenol 

Downstream Products

• 5378-52-9 phenyl-1H-tetrazole 
• 576-26-1 2.6-dimethylphenol 

Relevant academic research and scientific papers

Metal-assisted reactions. Part 26.1 Catalytic reactivity and ether bond lengths in aryloxytetrazoles and aryloxypseudosaccharins

X-Ray structure determinations on a variety of aryloxytetrazoles 1 and aryloxypseudosaccharins 4 have shown that the central C-O-C ether linkage is remarkable in having one very long C-O bond and one very short one. The central C-O-C bond angle is close t

Metal-assisted Reactions: Part 19. Burst Kinetics in Heterogeneous Catalytic Transfer Hydrogenolysis

Arene formation by catalytic transfer hydrogenolysis of aryloxytetrazolyl ethers in the liquid-phase shows biphasic concentration-time curves which indicate rate-limiting dissociation of heterogeneous complexes between catalyst and one of the reaction products, a tetrazolone.A dependence of catalytic reaction rate on pH and following modifications made to the catalyst are reported also.