Weight | 69.067 g/mol |
---|---|
Formula | C2H3N3 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
1H-1,2,3-Triazole (288-35-7, 288-36-8)
Score:
#1741 in Physics
,
#5424 in Chemistry
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- Sigma-Aldrich - 1H-1,2,3-Triazole48.40 - 178.00 USD
- Fisher Scientific - Search for 1H-1,2,3-Triazole
- TCI - 1H-1,2,3-Triazole125.00 - 436.00 USD
- Regulation of hydrogen peroxide in eye humors. Effect of 3-amino-1H-1,2,4-triazole on catalase and glutathione peroxidase of rabbit eye. (Biochimica et Biophysica Acta, 1977)
- Synthesis and Promising Properties of a New Family of High-Density Energetic Salts of 5-Nitro-3-trinitromethyl-1H-1,2,4-triazole and 5,5-Bis(trinitromethyl)-3,3-azo-1H-1,2,4-triazole (Journal of the American Chemical Society, 2011)
- Promotion of proton conduction in polymer electrolyte membranes by 1H-1,2,3-triazole. (Journal of the American Chemical Society, 2005)
- Synthesis, Biological Activity, and Molecular Modeling Studies of 1H-1,2,3-Triazole Derivatives of Carbohydrates as -Glucosidases Inhibitors (Journal of Medicinal Chemistry, 2010)
- Synthesis and in vitro characterization of 1-(4-aminofurazan-3-yl)-5-dialkylaminomethyl-1H-[1,2,3]triazole-4-carboxylic acid derivatives. A new class of selective GSK-3 inhibitors. (Journal of Medicinal Chemistry, 2003)
- Antiobesity effects of the novel in vivo neutral cannabinoid receptor antagonist 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-3-hexyl-1H-1,2,4-triazole - LH 21 (Neuropharmacology, 2006)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=NNN=C1
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InChIKeyQWENRTYMTSOGBR-UHFFFAOYSA-N
- Pubchem - 1H-1,2,3-Triazole
- Wikipedia - 1,2,3-Triazole
1,2,3-Triazole is one of a pair of isomeric chemical compounds with molecular formula C2H3N3, called triazoles, which have a five-membered ring of two carbon atoms and three nitrogen atoms. 1,2,3-Triazole is a basic aromatic heterocycle. Substituted 1,2,3-triazoles can be produced using the azide alkyne Huisgen cycloaddition in which an azide and an alkyne undergo a 1,3-dipolar cycloaddition reaction.
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