| Weight | 109.132 g/mol |
|---|---|
| Formula | C5H7N3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,6-Diaminopyridine (141-86-6)
pyridine-2,6-diamine
Score:
#2014 in Physics
,
#6287 in Chemistry
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- Importance of secondary interactions in triply hydrogen bonded complexes: guanine-cytosine vs uracil-2,6-diaminopyridine (Journal of the American Chemical Society, 1990)
- Synthesis and electron spin resonance studies of copper(II) complexes with acid amide derivatives of 2-amino and 2,6-diaminopyridine (Inorganica Chimica Acta, 1980)
- Derivatives of 2,6-diaminopyridine. (Journal of the American Chemical Society, 1947)
- Synthesis and spectroscopic structural investigations of the charge-transfer complexes formed in the reaction of 2,6-diaminopyridine with -acceptors TCNE, chloranil, and DDQ (Journal of Molecular Structure, 2007)
- Synthesis, crystal structure, antimicrobial activity and DNA-binding of hydrogen-bonded proton-transfer complex of 2,6-diaminopyridine with picric acid. (Journal of Photochemistry and Photobiology B-biology, 2011)
- Syntheses and electronic spectroscopy of [PtL(L')][ClO4] complexes (HL = 6-phenyl-2,2'-bipyridine; L' = pyridine, 4-aminopyridine, 2-aminopyridine, and 2,6-diaminopyridine). (Inorganic Chemistry, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - pyridine-2,6-diamine
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SMILESC1=CC(=NC(=C1)N)N
-
InChIKeyVHNQIURBCCNWDN-UHFFFAOYSA-N
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2,6-Diaminopyridine
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