5-Bromo-4-fluoro-2-pyridinamine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing nitrogen. The presence of bromine and fluorine substituents at the 5 and 4 positions, respectively, contributes to its unique chemical properties and reactivity. This compound typically exhibits moderate to high polarity due to the electronegative halogen atoms, which can influence its solubility in various solvents. It may participate in nucleophilic substitution reactions, particularly due to the amino group at the 2-position, which can act as a nucleophile. The compound's structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as halogenated pyridines are often found in biologically active compounds. Additionally, its specific reactivity and interactions can be influenced by the electronic effects of the bromine and fluorine substituents, making it a subject of interest in synthetic organic chemistry. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

5-Bromo-4-fluoro-2-pyridinamine

944401-69-8: 2-Amino-4-fluoro-5-bromopyridine, 2-Pyridinamine, 5-bromo-4-fluoro-, 5-Bromo-4-fluoro-2-pyridinamine, 5-Bromo-4-fluoropyridin-2-amine, 2-Amino-5-bromo-4-fluoropyridine

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CAS 944401-69-8: 5-Bromo-4-fluoro-2-pyridinamine

5-Bromo-4-fluoropyridin-2-amine

Ref: 3D-FB105195

5-bromo-4-fluoropyridin-2-amine

Ref: IN-DA00II67

5-Bromo-4-fluoropyridin-2-amine

Ref: 54-PC201380

5-Bromo-4-fluoropyridin-2-amine

Ref: 10-F220906