133638-20-7

Basic information

• Product Name: 1,1′-(1,2-phenylene)bis(1H-1,2,3,4-tetrazole)
• Synonyms: 1,1′-(1,2-phenylene)bis(1H-1,2,3,4-tetrazole)
• CAS NO: 133638-20-7
• Molecular Weight: 214.189
• Mol File: 133638-20-7.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1,1′-(1,2-phenylene)bis(1H-1,2,3,4-tetrazole)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1′-(1,2-phenylene)bis(1H-1,2,3,4-tetrazole)(133638-20-7)
• EPA Substance Registry System: 1,1′-(1,2-phenylene)bis(1H-1,2,3,4-tetrazole)(133638-20-7)

Safety Data

• Hazardous Substances Data: 133638-20-7(Hazardous Substances Data)

Upstream product

• 122-51-0 orthoformic acid triethyl ester 
• 95-54-5 1,2-diamino-benzene 
• 88-74-4 2-nitro-aniline 
• 14210-51-6 2-(tetrazol-1-yl)phenylamine 
• 14210-50-5 1-(2-nitrophenyl)-1H-1,2,3,4-tetrazole 

Relevant articles and documents

One-pot green synthesis of Cu/bone nanocomposite and its catalytic activity in the synthesis of 1-substituted 1H-1,2,3,4-tetrazoles and reduction of hazardous pollutants

In this work, a simple and green method is reported for the biosynthesis of Cu/bone nanocomposite using Cordyline fruticosa extract as a stabilizer and reductant. Animal bone was used as a natural support to prevent the accumulation of Cu nanoparticles. The catalytic activity of Cu/bone nanocomposite was assessed in the synthesis of 1-substituted 1H-1,2,3,4-tetrazoles and reduction of various organic dyes, including 4-nitrophenol (4-NP), nigrosin (NS), congo red (CR) and methylene blue (MB). The best catalytic performance in the synthesis of 1-substituted tetrazoles was achieved using 0.05?g of Cu/bone nanocomposite at 120°C. In addition, under optimal conditions, the absorption bands corresponding to 4-NP, CR, NS and MB completely disappeared after about 6?min, 3?min, 50?s and 7?s, respectively. The biosynthesis protocol used in the preparation of Cu/bone nanocomposite offers a very attractive area for further research.

Docking, Synthesis, Spectral Characterization, and Evaluation of In Vitro Antifungal Activity of Bis/Monophenyl-1-aryl-1H-tetrazole-5-carboxylate

Some novel compounds of bis/monophenyl-1-aryl-1H-tetrazole-5-carboxylate were synthesized by the equimolar reaction between bis/mono-1-aryl-1H-tetrazole and phenyl chloroformate in the presence of NaOH in dry tetrahydrofuran. The content was stirred for 4

Novel two step synthesis of bis/Mono 1-aryl-1H-tetrazole-5-carboxylic acid

Some novel compounds of bis/mono 1-aryl-1H-tetrazole-5-carboxylic acid are synthesized by the hydrolysis of two different synthesized esters, they are ethyl-1-aryl-1H-tetrazole-5-carboxylate and ethyloxo(1-aryl-1H-tetrazol-5-yl)acetate. The ethyl-1-aryl-1