| Weight | 112.092 g/mol |
|---|---|
| Formula | C3H4N4O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
1H-1,2,4-Triazole-3-carboxamide (3641-08-5)
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- Sigma-Aldrich - Search for 1H-1,2,4-Triazole-3-carboxamide
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- TCI - 1H-1,2,4-Triazole-3-carboxamide94.00 - 284.00 USD
- Design, synthesis, and in vitro biological evaluation of 1H-1,2,3-triazole-4-carboxamide derivatives as new anti-influenza A agents targeting virus nucleoprotein. (Journal of Medicinal Chemistry, 2012)
- Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide. (Journal of Agricultural and Food Chemistry, 2006)
- Preparation of 5-amino-1H,1,2,3-triazole-4-carboxamide. (Chemistry & Industry, 1970)
- Very-long-chain fatty acid biosynthesis is inhibited by cafenstrole, N,N-diethyl-3-mesitylsulfonyl-1H-1,2,4-triazole-1-carboxamide and its analogs. (Zeitschrift fr Naturforschung C, 2001)
- New solventless and metal-free synthesis of the antiepileptic drug 1-(2,6-difluorobenzyl)-1H-1,2,3-triazole-4-carboxamide (Rufinamide) and analogues (Tetrahedron Letters, 2015)
- 1H-1,2,4-triazole-3-carboxamide derivatives having cannabinoid-CB1 receptor agonistic, partial agonistic, inverse agonistic or antagonistic activity (2003)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=NNC(=N1)C(=O)N
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InChIKeyZEWJFUNFEABPGL-UHFFFAOYSA-N
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