CAS 121497-03-8
:TETRAZOLO[1,5-A]QUINOLINE-4-CARBALDEHYDE
Description:
Tetrazolo[1,5-a]quinoline-4-carbaldehyde is a heterocyclic organic compound characterized by its unique structure, which incorporates both a tetrazole and a quinoline moiety. This compound typically exhibits a range of interesting chemical properties due to the presence of the aldehyde functional group, which can participate in various chemical reactions, including condensation and nucleophilic addition. The tetrazole ring contributes to its potential as a bioactive molecule, as tetrazoles are known for their pharmacological properties. Tetrazolo[1,5-a]quinoline-4-carbaldehyde may also display fluorescence, making it useful in certain analytical applications. Its solubility can vary depending on the solvent, and it may be sensitive to light and moisture, necessitating careful handling and storage. The compound's reactivity and structural features make it a subject of interest in medicinal chemistry and materials science, where it may serve as a precursor for the synthesis of more complex molecules or as a building block in the development of new pharmaceuticals.
Formula:C10H6N4O
InChI:InChI=1/C10H6N4O/c15-6-8-5-7-3-1-2-4-9(7)14-10(8)11-12-13-14/h1-6H
SMILES:c1ccc2c(c1)cc(C=O)c1nnnn21
Synonyms:- Tetrazolo[1,5-a]quinoline-4-carboxaldehyde
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Found 2 products.
[1,2,3,4]Tetrazolo[1,5-a]quinoline-4-carbaldehyde
CAS:<p>1,2,3,4-Tetrazolo[1,5-a]quinoline-4-carbaldehyde is an imidazole derivative with antibacterial activity. It inhibits bacterial growth by binding to the β-unsaturated ketones in the cell wall and preventing their synthesis. 1,2,3,4-Tetrazolo[1,5-a]quinoline-4-carbaldehyde has been shown to be effective against Streptococcus mutans and other organisms. It is also a substrate for chlorination reactions and can be used as a catalyst in organic synthesis reactions.</p>Formula:C10H6N4OPurity:Min. 95%Molecular weight:198.18 g/mol

