CAS 1332324-22-7: 3,5-Dibromo-2-methoxy-4-methylpyridine

Description: 3,5-Dibromo-2-methoxy-4-methylpyridine is a heterocyclic organic compound characterized by its pyridine ring, which is substituted at the 2, 4, and 5 positions. The presence of two bromine atoms at the 3 and 5 positions contributes to its reactivity and potential applications in various chemical reactions, particularly in the synthesis of more complex molecules. The methoxy group at the 2-position enhances its solubility in organic solvents and may influence its electronic properties, while the methyl group at the 4-position can affect steric hindrance and reactivity. This compound is typically used in research and development, particularly in the fields of medicinal chemistry and agrochemicals, due to its potential biological activity. Its molecular structure suggests it may participate in nucleophilic substitution reactions, and its bromine substituents can serve as leaving groups in various synthetic pathways. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks.

Formula: C₇H₇Br₂NO

InChI: InChI=1S/C7H7Br2NO/c1-4-5(8)3-10-7(11-2)6(4)9/h3H,1-2H3

Pyridine, 3,5-dibromo-2-methoxy-4-methyl-

CAS: 1332324-22-7

• Formula: C₇H₇Br₂NO
• Purity: 97%
• Color and Shape: Solid
• Molecular weight: 280.9446

3,5-Dibromo-2-methoxy-4-methylpyridine

CAS: 1332324-22-7

• Purity: 95%
• Molecular weight: 280.94g/mol

3,5-Dibromo-2-methoxy-4-methylpyridine

CAS: 1332324-22-7

• Purity: 95.0%
• Molecular weight: 280.9469909667969

3,5-Dibromo-2-methoxy-4-methylpyridine

CAS: 1332324-22-7

Versatile small molecule scaffold

• Formula: C₇H₇Br₂NO
• Purity: Min. 95%
• Molecular weight: 280.95 g/mol