Pyridine, 2-bromo-3-methoxy-6-methyl-


Chemical Name: Pyridine, 2-bromo-3-methoxy-6-methyl-
CAS Number: 24207-22-5
Product Number: AG00BCKN(AGN-PC-0NDMCY)
Synonyms:
MDL No:
Molecular Formula: C7H8BrNO
Molecular Weight: 202.0485

Identification/Properties


Computed Properties
Molecular Weight:
202.051g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
200.979g/mol
Monoisotopic Mass:
200.979g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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NMR Spectrum


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Chemical Structure



2-Bromo-3-methoxy-6-methylpyridine, also known as $name$, is a versatile chemical compound commonly used in chemical synthesis processes. This compound serves as a valuable building block for the creation of various organic molecules due to its unique structural properties. In chemical synthesis, $name$ can act as a key intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals.One of the primary applications of 2-Bromo-3-methoxy-6-methylpyridine in chemical synthesis is its role as a functional group manipulator. The bromine atom and methoxy group present in the compound can undergo various reactions to introduce desired functional groups or modify existing ones in organic molecules. This versatility makes $name$ crucial in the development of complex organic compounds with specific chemical properties.Additionally, 2-Bromo-3-methoxy-6-methylpyridine can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling or Heck reaction, to form carbon-carbon or carbon-heteroatom bonds. These reactions are essential in building molecular frameworks found in pharmaceuticals, natural products, and advanced materials. By serving as a coupling partner, $name$ enables the synthesis of diverse chemical structures with high efficiency and precision.Furthermore, the presence of the pyridine ring in 2-Bromo-3-methoxy-6-methylpyridine makes it a valuable ligand in transition metal catalysis. The coordination ability of the pyridine moiety allows for the formation of stable complexes with various metal catalysts, enhancing their reactivity and selectivity in organic transformations. This capability makes $name$ a crucial component in catalytic processes for synthesizing complex molecules with high stereoselectivity and yield.In conclusion, 2-Bromo-3-methoxy-6-methylpyridine plays a pivotal role in chemical synthesis by serving as a versatile building block, functional group manipulator, coupling partner, and ligand in diverse synthetic transformations. Its applications extend to the development of pharmaceuticals, agrochemicals, and fine chemicals, highlighting its significance in modern organic chemistry practices.