2-(2H-Tetrazol-5-yl)-ethanol is an organic compound characterized by the presence of a tetrazole ring, which is a five-membered heterocyclic structure containing four nitrogen atoms and one carbon atom. This compound features an ethanol moiety, indicating the presence of a hydroxyl (-OH) group attached to a two-carbon ethyl chain. The tetrazole ring contributes to the compound's potential biological activity, as tetrazoles are known for their ability to act as bioisosteres of carboxylic acids and can participate in various chemical reactions, including nucleophilic substitutions and cycloadditions. The presence of the hydroxyl group enhances its solubility in polar solvents and may influence its reactivity and interaction with biological systems. Additionally, 2-(2H-tetrazol-5-yl)-ethanol may exhibit properties such as being a potential ligand in coordination chemistry or a precursor in the synthesis of other tetrazole derivatives. Its applications can span pharmaceuticals, agrochemicals, and materials science, depending on its specific reactivity and functionalization.

2-(2H-TETRAZOL-5-YL)-ETHANOL

17587-08-5: 2-(2H-Tetrazol-5-yl)-ethanol is an organic compound characterized by the presence of a tetrazole ring, which is a five-membered heterocyclic structure containing four nitrogen atoms and one carbon atom. This compound features an ethanol moiety, indicating the presence of a hydroxyl (-OH) group attached to a two-carbon ethyl chain. The tetrazole ring contributes to the compound's potential biological activity, as tetrazoles are known for their ability to act as bioisosteres of carboxylic acids and can participate in various chemical reactions, including nucleophilic substitutions and cycloadditions. The presence of the hydroxyl group enhances its solubility in polar solvents and may influence its reactivity and interaction with biological systems. Additionally, 2-(2H-tetrazol-5-yl)-ethanol may exhibit properties such as being a potential ligand in coordination chemistry or a precursor in the synthesis of other tetrazole derivatives. Its applications can span pharmaceuticals, agrochemicals, and materials science, depending on its specific reactivity and functionalization.

CAS 17587-08-5

2-(2H-TETRAZOL-5-YL)-ETHANOL

2H-Tetrazole-5-ethanol

Ref: IN-DA00218Y

2-(1H-tetrazol-5-yl)ethanol

Ref: 10-F309306