| Weight | 95.105 g/mol |
|---|---|
| Formula | C4H5N3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2-Aminopyrazine (5049-61-6)
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- Synthesis, characterization, spectroscopic and photophysical studies of ternary complexes of Eu(III) with 3-aminopyrazine-2-carboxylic acid (HL) and heterobiaryl ligands (2,2-bipyridine and 1,10-phenanthroline) (Journal of Alloys and Compounds, 1993)
- Crystal structures and magnetic properties of Mn[N(CN)2]2L (L = 2,5-dimethylpyrazine and aminopyrazine) (Polyhedron, 2001)
- Syntheses, structures, photoluminescences of silver(I) coordination polymers with 2-aminopyrazine and varied dicarboxylate ligands (Polyhedron, 2010)
- Pteridines. XVI. A Synthesis of 2-Aminopyrazine-3-carboxamides by Reductive Ring Cleavage of 3-Hydroxy-1-pyrazolo [b] pyrazines1-3 (Journal of the American Chemical Society, 1958)
- TMSCl-Promoted Isocyanide-Based MCR of Ethylenediamines: An Efficient Assembling of 2-Aminopyrazine Core. (Tetrahedron Letters, 2007)
- Synthesis, characterization and anticancer activity of 3-aminopyrazine-2-carboxylic acid transition metal complexes (Transition Metal Chemistry, 2009)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CN=C(C=N1)N
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InChIKeyXFTQRUTUGRCSGO-UHFFFAOYSA-N
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2-Aminopyrazine
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