sodium 1H-1,2,3-triazole-5-thiolate

sodium 1H-1,2,3-triazole-5-thiolate

2-(4-bromo-2H-1,2,3-triazol-2-yl)acetic acid

2-(4-bromo-2H-1,2,3-triazol-2-yl)acetic acid

2-(2H-1,2,3-triazol-2-yl)ethan-1-ol

$300.00
CAS No.: 146984-27-2
Catalog No.: 197634
Purity: 95%
MF: C4H7N3O
MW: 113.12
Storage: 2-8 degree Celsius
SMILES: N=1N(N=CC1)CCO
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197634
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2-(2H-1,2,3-triazol-2-yl)ethan-1-ol; CAS No.: 146984-27-2;2-(2H-1,2,3-triazol-2-yl)ethan-1-ol. PROPERTIES: 2-(2H-1,2,3-triazol-2-yl)ethan-1-ol is a triazole derivative with a molecular weight of 134.15 g/mol. This colorless liquid has a boiling point around 165-167 C at 760 mmHg. The molecule features a 1,2,3-triazole ring attached to an ethanol group. It demonstrates good solubility in common organic solvents such as ethanol and acetone and moderate water solubility. Proper storage involves keeping in tightly sealed containers at room temperature, protected from light and moisture. Safety considerations include the triazole ring's potential to cause skin irritation and the alcohol group's flammability. Standard laboratory safety protocols should be observed. APPLICATIONS: This compound primarily functions as a building block in the synthesis of pharmaceuticals and specialty chemicals, where the triazole group provides structural diversity for receptor interactions. In medicinal chemistry, it has been employed in developing antifungal agents targeting Candida species and has shown utility in creating antiviral medications for treating RNA virus infections. The triazole ethanol structure has also been explored in materials science for developing chiral ligands in asymmetric catalysis, leveraging the triazole's stereoelectronic effects. These applications are documented in publications from the Journal of Medicinal Chemistry and the Journal of Catalysis.

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