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Home  > 4-Bromo-2-methoxy-6-methylpyridine

AD77837

1083169-00-9 | 4-Bromo-2-methoxy-6-methylpyridine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $67.00 $47.00 -   +
250mg 95% in stock $146.00 $102.00 -   +
1g 95% in stock $344.00 $241.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AD77837
Chemical Name: 4-Bromo-2-methoxy-6-methylpyridine
CAS Number: 1083169-00-9
Molecular Formula: C7H8BrNO
Molecular Weight: 202.04851999999997
MDL Number: MFCD16610113
SMILES: COc1cc(Br)cc(n1)C

 

Upstream Synthesis Route
  • 4-Bromo-2-methoxy-6-methylpyridine is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in organic synthesis, particularly in the pharmaceutical industry, where it is utilized in the preparation of various drug candidates and active pharmaceutical ingredients.One of the key applications of 4-Bromo-2-methoxy-6-methylpyridine is its role as a nucleophilic and electrophilic reagent in cross-coupling reactions. It can participate in Suzuki-Miyaura cross-coupling reactions with aryl or heteroaryl boronic acids to form biaryl compounds, which are important structural motifs found in many pharmaceuticals and agrochemicals. Additionally, this compound can be utilized in Buchwald-Hartwig amination reactions to introduce nitrogen-containing functional groups into organic molecules.Furthermore, 4-Bromo-2-methoxy-6-methylpyridine can serve as a key intermediate in the synthesis of various heterocyclic compounds, which are prevalent in drug design and medicinal chemistry. Its unique substitution pattern and electron density allow for selective functionalization and regioselective reactions, making it a valuable tool in the construction of complex organic molecules.In summary, 4-Bromo-2-methoxy-6-methylpyridine plays a crucial role in chemical synthesis by enabling the efficient construction of diverse organic compounds, particularly in the development of pharmaceuticals and biologically active molecules.
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