14210-30-1

Upstream product

• 14210-25-4 5-Chloro-1-phenyltetrazole 

Downstream Products

• 14210-33-4 1-(4-aminophenyl)-5-chlorotetrazole 
• 111969-11-0 5-(4-Methoxy-phenoxy)-1-(4-nitro-phenyl)-1H-tetrazole 
• 14213-13-9 4-tetrazol-1-yl-phenylamine 
• 191594-10-2 5-(cinnamyloxy)-1-(4-nitrophenyl)-1H-tetrazole 
• 111969-10-9 4-[5-(4-Methoxy-phenoxy)-tetrazol-1-yl]-phenylamine 
• 191594-11-3 4-(5-(cinnamyloxy)-1H-tetrazol-1-yl)aniline 

Relevant academic research and scientific papers

Preparation and characterization of novel side-chain azobenzene polymers containing tetrazole group

A novel methacrylate monomer containing azobenzene chromophore and tetrazole moiety, 4′-(2-methacryloxyethyl)methylamino-4-(5-chlorotetrazol-1-yl)azobenzene (MACA), was synthesized and polymerized to form homopolymer (PMACA) via reversible addition-fragme

NOVEL SULFONAMIDE SUBSTITUTED CHROMAN DERIVATIVES USEFUL AS BETA-3 ADRENORECEPTOR AGONISTS

This invention relates to novel sulfonamide substituted chroman derivatives which are useful in the treatment of beta-3 receptor mediated conditions.

SULFONAMIDE SUBSTITUTED CHROMAN DERIVATIVES USEFUL AS BETA 3 ADRENORECEPTOR AGONISTS

This invention related to novel sulfonamide substituted chroman derivatives which are useful in the treatment of beta-3 receptor mediated conditions.

A kinetic investigation of the thermal rearrangement of allyloxytetrazoles to N-allyltetrazolones

The mechanism of the thermal rearrangement of 1-aryl-5-allyloxytetrazoles 1 to give 1-aryl-4-allyltetrazolones 2 in very high yield has been investigated through kinetic studies in one polar and one less polar solvent. The results suggest mainly a concerted [3,3] sigmatropic process, in which a partially positively charged allyl group migrates from oxygen to nitrogen, similar to the polar transition state found in the Claisen rearrangement.

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.