3544-13-6

Basic information

• Product Name: 5,5’-(1,3-phenylene)bis(1H-tetrazole)
• Synonyms: 5,5’-(1,3-phenylene)bis(1H-tetrazole)
• CAS NO: 3544-13-6
• Molecular Weight: 214.189
• Mol File: 3544-13-6.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 5,5’-(1,3-phenylene)bis(1H-tetrazole)(CAS DataBase Reference)
• NIST Chemistry Reference: 5,5’-(1,3-phenylene)bis(1H-tetrazole)(3544-13-6)
• EPA Substance Registry System: 5,5’-(1,3-phenylene)bis(1H-tetrazole)(3544-13-6)

Safety Data

• Hazardous Substances Data: 3544-13-6(Hazardous Substances Data)

Upstream product

• 176636-07-0 2,2'-bis(tributylstannyl)-5,5'-m-phenylenebis(tetrazole) 
• 626-17-5 benzene-1,3-dicarbonitrile 

Downstream Products

• 191339-66-9 1,3-Bis[2-(6-bromohexyl)tetrazol-5-yl]benzene 
• 191339-65-8 1,3-Bis[2-(8-bromooctyl)tetrazol-5-yl]benzene 
• 1383847-57-1 5-phenyl-2-(6-(5-(3-(2-(6-(5-phenyl-2H-tetrazol-2-yl)hexyl)-2H-tetrazol-5-yl)phenyl)-2H-tetrazol-2-yl)hexyl)-2H-tetrazole 
• 1383847-58-2 5-phenyl-2-(6-(5-(3-(1-(6-(5-phenyl-2H-tetrazol-2-yl)hexyl)-1H-tetrazol-5-yl)phenyl)-2H-tetrazol-2-yl)hexyl)-2H-tetrazole 
• 1383847-59-3 2-(2-(6-(5-(3-(2-(6-(5-(pyridin-2-yl)-2H-tetrazol-2-yl)hexyl)-2H-tetrazol-5-yl)phenyl)-2H-tetrazol-2-yl)-2H-tetrazol-5-yl))pyridine 
• 1354833-31-0 1,2-bis{5-[3-(2-vinyl-2H-tetrazol-5-yl)phenyl]-2H-tetrazol-2-yl}ethane 
• 1210461-16-7 [Cd(1,3-di(2H-1,2,3,4-tetrazol-5-yl)benzene^(2-))(H₂O)(1,10-phenanthroline)] 

Relevant articles and documents

Two SrII coordination compounds based on tetrazole-carboxylate ligands

Two novel coordination compounds, [Sr(atzp)2(H2O)2]·CH3OH (1) and [Sr(dtzpha)(H2O)3]·4H2O (2) [Hatzp=5-aminotetrazole-1-propionic acid, H2dtzpha=1,3-di(tetrazol-5-yl)benzene-N2,N2'-diacetic acid)], have been generated by using 5-aminotetrazole-1-propionic acid and 1,3-di(tetrazol-5-yl)benzene-N2,N2'-diacetic acid to react with strontium salts, respectively. X-ray diffraction analysis reveals that carboxylic groups of two ligands show the same coordination mode (the μ1,1,3-COO coordination mode), compound 1 displays a 1D structure while compound 2 shows a 2D structure, which implies the influence of the number of the carboxylic acid groups. Luminescence properties of 1 and 2 were investigated at room temperature in the solid state.

Biosynthesis of Pd/MnO2 nanocomposite using Solanum melongena plant extract and its application for the one-pot synthesis of 5-substituted 1H-tetrazoles from aryl halides

In this work, for the first time, Solanum melongena plant extract was used for the green synthesis of Pd/MnO2 nanocomposite via reduction osf Pd(II) ions to Pd(0) and their immobilization on the surface of manganese dioxide (MnO2) nanoparticles (NPs) as an effective support. The synthesized nanocomposite were characterized by various analytical techniques such as Fourier transform infrared (FT-IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDS) and UV–Vis spectroscopy. The catalytic activity of Pd/MnO2 nanocomposite was used as a heterogeneous catalyst for the one-pot synthesis of 5-substituted 1H-tetrazoles from aryl halides containing various electron-donating or electron-withdrawing groups in the presence of K4[Fe (CN)6] as non-toxic cyanide source and sodium azide. The products were obtained in good yields via a simple methodology and easy work-up. The nanocatalyst can be recycled and reused several times with no remarkable loss of activity.

Synthesis of 5-substituted 1H-tetrazoles from aryl halides using nanopolymer-anchored palladium(II) complex as a new heterogeneous and reusable catalyst

Abstract: This paper reports on the preparation and use of chloromethylated polystyrene-anchored palladium(II) complex, [Ps-ttet-Pd(II)], as a separable nanocatalyst for the synthesis of 5-substituted 1H-tetrazoles by treating aryl halides with K4[Fe(CN)6] as non-toxic cyanide source, to generate in situ the corresponding aryl nitriles which then react through [2?+?3] cycloaddition with sodium azide. High yields of the products, simple methodology, easy work-up procedure, high catalytic activity, and superior cycling stability of the catalyst are the main advantages of this protocol. The structure of the catalyst was characterized using the powder XRD, SEM, TG-DTA, EDS, AAS, and FT-IR spectroscopy techniques. Graphical abstract: [Figure not available: see fulltext.]