CAS 524718-27-2

4-Bromo-6-methyl-2-pyridinamine

Description:

4-Bromo-6-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 4-position and a methyl group at the 6-position of the pyridine ring contributes to its unique chemical properties. This compound typically exhibits moderate solubility in polar solvents due to the presence of the amino group, which can engage in hydrogen bonding. Its molecular structure suggests potential reactivity, particularly in nucleophilic substitution reactions, owing to the electron-withdrawing nature of the bromine substituent. Additionally, the amino group can participate in various chemical transformations, making it a valuable intermediate in organic synthesis. The compound may also exhibit biological activity, which can be explored in medicinal chemistry contexts. Overall, 4-Bromo-6-methyl-2-pyridinamine is a versatile compound with applications in research and development, particularly in the fields of pharmaceuticals and agrochemicals.

Formula: C₆H₇BrN₂

Synonyms:

• 4-Bromo-6-Methylpyridin-2-Amine

4-Bromo-6-methylpyridin-2-amine

CAS: 524718-27-2

Formula: C₆H₇BrN₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 187.0372

Ref: IN-DA0038OJ

4-Bromo-6-methylpyridin-2-amine

CAS: 524718-27-2

4-Bromo-6-methylpyridin-2-amine

Purity: 97%

Molecular weight: 187.04g/mol

Ref: 54-OR948239

4-Bromo-6-methylpyridin-2-amine

CAS: 524718-27-2

Formula: C₆H₇BrN₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 187.04

Ref: 10-F230995

4-Bromo-6-methyl-2-pyridinamine

CAS: 524718-27-2

4-Bromo-6-methyl-2-pyridinamine is a small molecule that binds to the bromodomain of the human protein BRD4. This binding inhibits the interaction between BRD4 and acetylated lysine residues on histones, thereby inhibiting transcriptional activation. 4-Bromo-6-methyl-2-pyridinamine has been shown to be a potent inhibitor of the activity of BRD4, which may be due to its chemical stability and ability to inhibit protein synthesis. The compound's potency in inhibition assays and its lack of biochemical toxicity make it an attractive lead compound for further study.

Formula: C₆H₇BrN₂

Purity: Min. 95%

Molecular weight: 187.04 g/mol

Ref: 3D-FB138870