CAS 14506-41-3
:phenyl(2H-tetrazol-5-yl)methanone
Description:
Phenyl(2H-tetrazol-5-yl)methanone, with the CAS number 14506-41-3, is an organic compound characterized by the presence of a phenyl group and a tetrazole ring. The tetrazole moiety contributes to its potential as a bioactive compound, often exhibiting properties such as antimicrobial and antifungal activities. This compound typically appears as a solid at room temperature and is soluble in polar organic solvents. Its structure includes a carbonyl group (ketone) linked to the tetrazole, which can influence its reactivity and interactions with other molecules. The presence of the tetrazole ring also suggests potential applications in pharmaceuticals, particularly in drug design, due to its ability to mimic carboxylic acids and its involvement in hydrogen bonding. Additionally, the compound may exhibit interesting electronic properties due to the conjugation between the phenyl and tetrazole groups, making it a subject of interest in materials science and organic synthesis. Overall, phenyl(2H-tetrazol-5-yl)methanone is a versatile compound with potential applications across various fields.
Formula:C8H6N4O
InChI:InChI=1/C8H6N4O/c13-7(8-9-11-12-10-8)6-4-2-1-3-5-6/h1-5H,(H,9,10,11,12)
SMILES:c1ccc(cc1)C(=O)c1n[nH]nn1
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Found 3 products.
5-Benzoyl-2H-1,2,3,4-tetrazole
CAS:Controlled Product<p>Applications 5-benzoyl-2H-1,2,3,4-tetrazole (cas# 14506-41-3) is a useful research chemical.<br></p>Formula:C8H6N4OColor and Shape:NeatMolecular weight:174.1595-Benzoyl-2H-1,2,3,4-tetrazole
CAS:<p>5-Benzoyl-2H-1,2,3,4-tetrazole is a pyrazole compound that can be synthesized by reacting an aliphatic azide with a sulfoxide. The reaction of the sulfoxide with potassium hydroxide and dimethylbenzoyl chloride produces the desired product. 5-Benzoyl-2H-1,2,3,4-tetrazole is used in research as a short term substrate for enzymes such as diazo compounds and tetrazole. It has also been shown to be capable of forming covalent bonds with alkali metal ions such as sodium and potassium. This compound is also useful for the synthesis of 2H-1,2,3,4-tetrazoles via diazotization.</p>Formula:C8H6N4OPurity:Min. 95%Molecular weight:174.16 g/mol


