CAS 89466-17-1

6-Bromo-5-methyl-2-pyridinamine

Description:

6-Bromo-5-methyl-2-pyridinamine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a bromine atom at the 6-position and a methyl group at the 5-position of the pyridine ring contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino group, which can engage in hydrogen bonding. The amino group also makes it a potential candidate for further chemical modifications and applications in pharmaceuticals or agrochemicals. Its reactivity can be influenced by the electron-withdrawing nature of the bromine atom, which can affect nucleophilic substitution reactions. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks.

Formula: C₆H₇BrN₂

InChI: InChI=1S/C6H7BrN2/c1-4-2-3-5(8)9-6(4)7/h2-3H,1H3,(H2,8,9)

InChI key: InChIKey=DDCMBKXJOGOCPM-UHFFFAOYSA-N

SMILES: BrC1=C(C)C=CC(N)=N1

Synonyms:

• 2-Pyridinamine, 6-bromo-5-methyl-
• 3-Picoline, 6-amino-2-bromo-
• 6-BroMo-5-Methyl-2-pyridinaMine

6-Bromo-5-Methyl-2-Pyridinamine

CAS: 89466-17-1

Formula: C₆H₇BrN₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 187.0372

Ref: IN-DA00H0YV

6-Bromo-5-methyl-2-pyridinamine

CAS: 89466-17-1

6-Bromo-5-methyl-2-pyridinamine

Purity: 98%

Molecular weight: 187.04g/mol

Ref: 54-OR71183

6-Bromo-5-methylpyridin-2-amine

CAS: 89466-17-1

Formula: C₆H₇BrN₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 187.04

Ref: 10-F338605

6-bromo-5-methylpyridin-2-amine

CAS: 89466-17-1

6-Bromo-5-methylpyridin-2-amine is an imidazopyridine drug that has been shown to inhibit the growth of bacterial strains in vitro. It also binds to the electron density, which may be due to its heteroaromatic ring and ionization potential. 6BMPA is synthesized by reacting 2-chloro-6-bromopyridine with 5-methylpyridinium iodide. For the synthesis of a monomer, 6BMPA is reacted with a second molecule of 5-methylpyridinium iodide, yielding the imidazopyrazine as a product. Drug discovery for this compound has been shown to be promising in animal models.

Formula: C₆H₇BrN₂

Purity: Min. 95%

Molecular weight: 187 g/mol

Ref: 3D-PDA46617