Weight | 109.132 g/mol |
---|---|
Formula | C5H7N3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
2,5-DIAMINOPYRIDINE (4318-76-7)
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- Synthesis, spectroscopic characterization and structural investigations of a new charge transfer complex of 2,6-diaminopyridine with 3,5-dinitrobenzoic acid: DNA binding and antimicrobial studies (Journal of Molecular Structure, 2013)
- Changes in cytosolic free calcium with 1,2,3,4-tetrahydro-5-aminoacridine, 4-aminopyridine and 3,4-diaminopyridine. (Biochemical Pharmacology, 1988)
- Synergistic effect of tartaric acid with 2,6-diaminopyridine on the corrosion inhibition of mild steel in 0.5 M HCl (Scientific Reports, 2016)
- Synthesis and Characterization of a Novel Unsymmetrical Tetradentate Schiff Base Complex of Zinc(II) Derived from N,N-bis (5-Bromosalicylidene) 2,3-Diaminopyridine (H2L): Crystal Structure of [Zn(II)L]Pyridine (Journal of Chemical Crystallography, 2010)
- Preparation of pyrazolo [1,5-a]pyridine and [1,2,4]triazolo[1,5-a]pyridine derivatives from 1,6-diaminopyridine-2-thiones (Heterocycles, 1988)
- Experimental and Theoretical Studies on the Functionalization Reactions of 4-Benzoyl-1,5-Diphenyl-1H-Pyrazole-3-Carboxylic Acid and Acid Chloride with 2,3-Diaminopyridine (Molecules, 2005)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=NC=C1N)N
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InChIKeyMIROPXUFDXCYLG-UHFFFAOYSA-N
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