CAS 84249-14-9
:2-amino-4-bromopyridine
Description:
2-Amino-4-bromopyridine is an organic compound characterized by a pyridine ring substituted with an amino group and a bromine atom. Its molecular formula is C5H5BrN2, indicating the presence of five carbon atoms, five hydrogen atoms, one bromine atom, and two nitrogen atoms. This compound typically appears as a solid at room temperature and is soluble in polar solvents such as water and alcohols, owing to the presence of the amino group, which can engage in hydrogen bonding. The bromine substituent introduces a degree of electrophilicity, making it a useful intermediate in various organic synthesis reactions, including nucleophilic substitutions and coupling reactions. Additionally, 2-amino-4-bromopyridine can exhibit biological activity, making it of interest in pharmaceutical research. Its properties, such as melting point and boiling point, can vary based on purity and environmental conditions. As with many brominated compounds, it is essential to handle it with care due to potential toxicity and environmental impact.
Formula:C5H5BrN2
Synonyms:- 4-Bromo-2-aminopyridine
- 4-Bromo-2-amine-pyridin
- 4-Bromo-2-pyridinamine
- 2-Amino-4-bromo pyridine
- 4-Bromopyridine-2-amine
- 4-Bromopyridin-2-Amine
- 4-Bromo-Pyridin-2-Ylamine
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Found 7 products.
2-Amino-4-bromopyridine
CAS:Formula:C5H5BrN2Purity:>98.0%(GC)(T)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:173.012-Amino-4-bromopyridine
CAS:2-Amino-4-bromopyridineFormula:C5H5BrN2Purity:95%Color and Shape: white solidMolecular weight:173.01g/mol2-Amino-4-bromopyridine
CAS:Formula:C5H5BrN2Purity:96%Color and Shape:Solid, Crystalline PowderMolecular weight:173.0132-Amino-4-bromopyridine
CAS:Controlled ProductFormula:C5H5BrN2Color and Shape:Off-White To BeigeMolecular weight:173.012-Amino-4-bromopyridine
CAS:<p>2-Amino-4-bromopyridine is a potent, selective antagonist of the nicotinic acetylcholine receptor (nAChR) that has been shown to inhibit the proliferation of cancer cells in vitro. 2-Amino-4-bromopyridine binds to the nAChR and stabilizes it by binding to an allosteric site on the receptor. 2-Amino-4-bromopyridine is synthesized from 4,5-dibromobenzene and 2,6-diaminopyridine in two steps with a yield of 47%. The synthesis of 2-amino-4-bromopyridine proceeds via reaction mechanism involving electrophilic substitution at the bromine atom followed by nucleophilic addition at the nitrogen atom.</p>Formula:C5H5BrN2Purity:Min. 95%Color and Shape:PowderMolecular weight:173.01 g/mol






