| Weight | 108.144 g/mol |
|---|---|
| Formula | C6H8N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
3-Amino-4-methylpyridine (3430-27-1)
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- J(Pt,H) and Pt.cntdot..cntdot..cntdot.H-C interactions in Schiff base complexes of 2-(benzylideneamino)-3-methylpyridine. Molecular structures of dichloro(2-((2,4,6-trimethylbenzylidene)amino)-3-methylpyridine)(triethylarsine)platinum(II) and dichloro(2-amino-3-methylpyridine)(triethylphosphine)palladium(II) (Inorganic Chemistry, 1987)
- Syntheses and Antitumor Activities of Potent Inhibitors of Ribonucleotide Reductase: 3-Amino-4-Methylpyridine-2-Carboxaldehyde-Thiosemicarbazone (3-Amp), 3-Amino-Pyridine-2-Carboxaldehyde-Thiosemicarbazone (3-Ap) and its Water-Soluble Prodrugs (Current Medicinal Chemistry, 2001)
- One-dimensional oxalato-bridged copper(II) complexes with 3-hydroxypyridine and 2-amino-4-methylpyridine (Inorganica Chimica Acta, 2001)
- Molecular and crystal structures, vibrational studies and quantum chemical calculations of 3 and 5-nitroderivatives of 2-amino-4-methylpyridine (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2012)
- Cyclic and open-chain tautomerism and complex formation behaviour of the condensation product of 2-amino-3-aminomethyl-4-methoxymethyl-6-methylpyridine with salicylaldehyde (Polyhedron, 1985)
- Efficient synthesis of ribonucleotide reductase inhibitors 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP) and 3-amino-4-methylpyridine-2-carboxaldehyde thiosemicarbazone (3-AMP) via palladium mediated cross-coupling reactions (Tetrahedron, 1998)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=C(C=NC=C1)N
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InChIKeyIBKMZYWDWWIWEL-UHFFFAOYSA-N
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