| Weight | 109.132 g/mol |
|---|---|
| Formula | C5H7N3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,3-Diaminopyridine (452-58-4)
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- Synthesis and Anti-Bacterial/Catalytic Properties of Schiff Bases and Schiff Base Metal Complexes Derived from 2,3-Diaminopyridine (Synthesis and Reactivity in Inorganic and Metal-organic Chemistry, 2000)
- Synthesis, characterization and redox properties of macrocyclic Schiff base by reaction of 2,6-diaminopyridine and 1,3-bis(2-carboxyaldehyde phenoxy)propane and its CuII, NiII, PbII, CoIII and LaIII complexes (Transition Metal Chemistry, 2007)
- 2,3-diaminopyridine bradykinin B1 receptor antagonists. (Journal of Medicinal Chemistry, 2004)
- 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)
- Erratum: Schiff base substitute polyphenol and its metal complexes derived from ovanillin with 2,3diaminopyridine: synthesis, characterization, thermal, and conductivity properties (Polymers for Advanced Technologies, 2008)
- Spectroscopic studies of the reaction of iodine with 2,3-diaminopyridine. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C(N=C1)N)N
-
InChIKeyZZYXNRREDYWPLN-UHFFFAOYSA-N
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2,3-Diaminopyridine
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