| Weight | 173.013 g/mol |
|---|---|
| Formula | C5H5BrN2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2-Amino-6-bromopyridine (19798-81-3)
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- Electrocatalytic carboxylation of 2-amino-5-bromopyridine with CO2 in ionic liquid 1-butyl-3-methyllimidazoliumtetrafluoborate to 6-aminonicotinic acid (Electrochimica Acta, 2010)
- An unexpected result in the condensation of 2amino6bromopyridine with ethyl 4chloroacetoacetate: Four dihalosubstituted pyrido[1,2a]pyrimidin4ones as reaction products (Journal of Heterocyclic Chemistry, 1999)
- Synthesis of 2-Amino-6-bromopyridine (Chemistry World, 2010)
- ChemInform Abstract: An Unexpected Result in the Condensation of 2Amino6bromopyridine with Ethyl 4Chloroacetoacetate: Four DihaloSubstituted Pyrido[1,2a]pyrimidin4ones as Reaction Products. (ChemInform, 2010)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=NC(=C1)Br)N
-
InChIKeyBKLJUYPLUWUEOQ-UHFFFAOYSA-N
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