6926-49-4

Basic information

• Product Name: 5-[4-(2H-tetrazol-5-yl)phenyl]-2H-tetrazole
• Synonyms: 5-[4-(2H-tetrazol-5-yl)phenyl]-2H-tetrazole
• CAS NO: 6926-49-4
• Molecular Formula: C₈H₆N₈
• Molecular Weight: 214.18684
• EINECS: -0
• Mol File: 6926-49-4.mol
• Article Data: 28

Chemical Properties

• Melting Point: 296-297 °C (decomp)
• Boiling Point: 539.1°Cat760mmHg
• Flash Point: 269.5°C
• Appearance: /
• Density: 1.575g/cm³
• PKA: 3.63±0.10(Predicted)
• CAS DataBase Reference: 5-[4-(2H-tetrazol-5-yl)phenyl]-2H-tetrazole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-[4-(2H-tetrazol-5-yl)phenyl]-2H-tetrazole(6926-49-4)
• EPA Substance Registry System: 5-[4-(2H-tetrazol-5-yl)phenyl]-2H-tetrazole(6926-49-4)

Safety Data

• Hazardous Substances Data: 6926-49-4(Hazardous Substances Data)

Usage

General Description

5-[4-(2H-tetrazol-5-yl)phenyl]-2H-tetrazole is a chemical compound with a molecular formula of C8H6N10. It is a tetrazole derivative that contains two tetrazole rings and a phenyl group. Tetrazoles are a class of organic compounds that contain a five-membered ring with four nitrogen atoms and are known for their diverse range of biological and pharmacological activities. This particular compound may have potential applications in pharmaceuticals as a building block for synthesizing new drugs or as a ligand in coordination chemistry due to its unique structure and properties. However, further research and testing would be necessary to determine its specific uses and properties.

Upstream product

• 623-26-7 terephthalonitrile 
• 176636-08-1 2,2'-bis(tributylstannyl)-5,5'-p-phenylenebis(tetrazole) 
• 14389-10-7 5-(4-cyanophenyl)-2H-tetrazole 
• 106-37-6 1.4-dibromobenzene 
• 624-38-4 para-diiodobenzene 
• 52707-54-7 4-cyanobenzaldehyde oxime 
• 623-27-8 terephthalaldehyde, 

Downstream Products

• 100137-06-2 5,5'-dimethyl-2,2'-p-phenylene-bis-[1,3,4]oxadiazole 

Relevant articles and documents

Tetrazoles: A new class of compound for crystallization modification

Tetrazoles are a class of organic compound often used as carboxylic acid analogues. This analogous behaviour is shown to extend to crystallization modification, that is, tetrazoles are also able to influence crystal growth and morphology although in a dif

CuO–NiO bimetallic nanoparticles supported on graphitic carbon nitride with enhanced catalytic performance for the synthesis of 1,2,3-triazoles, bis-1,2,3-triazoles, and tetrazoles in parts per million level

The unification of CuCl2·2H2O and NiCl2·6H2O with the support of graphitic carbon nitride yielded to form an efficient, synergistic, bimetallic nano-catalyst CuO–NiO@g-C3N4. FT-IR, SEM, TEM

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.

Tandem magnetization and post-synthetic metal ion exchange of metal–organic framework: Synthesis, characterization and catalytic study

For the first time, metal-exchange in a magnetic metal–organic framework (MOF) via tandem magnetization and post-synthetic modification has been developed. The new magnetic mixed-metal metal–organic framework nanocomposite, CoFe2O4/[