Weight | 138.126 g/mol |
---|---|
Formula | C6H6N2O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
2-Aminonicotinic acid (5345-47-1)
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- Molecular structure (monomeric and dimeric structure) and HOMO-LUMO analysis of 2-aminonicotinic acid: a comparison of calculated spectroscopic properties with FT-IR and UV-vis. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2012)
- Electroorganic synthesis of 6-aminonicotinic acid from 2-amino-5-chloropyridine (Tetrahedron Letters, 2003)
- Isothiazoles. Part 11: 3-Azahexatrienes from 2-Arylpropenamidines: Electrocyclization to 6-Aminonicotinic Acid Derivatives (Tetrahedron, 2000)
- Electrocatalytic carboxylation of 2-amino-5-bromopyridine with CO2 in ionic liquid 1-butyl-3-methyllimidazoliumtetrafluoborate to 6-aminonicotinic acid (Electrochimica Acta, 2010)
- Chemoselective cyclization of aminonicotinic acid derivatives to 1,8-naphthyridin-2-ones via a potential intramolecular azadiene-ketene electrocyclization reaction. (Journal of Organic Chemistry, 2001)
- Synthesis and psychotropic activity of amides of 2-aminonicotinic acid (Pharmaceutical Chemistry Journal, 1986)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C(N=C1)N)C(=O)O
-
InChIKeyKPIVDNYJNOPGBE-UHFFFAOYSA-N
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