1142192-55-9 | Methyl 5-bromo-3-methoxypicolinate

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$58.00	$41.00
1g	95%	in stock	$134.00	$94.00
10g	95%	in stock	$1,226.00	$858.00
25g	95%	in stock	$2,414.00	$1,690.00

Description

• Catalog Number: AA13862
• Chemical Name: Methyl 5-bromo-3-methoxypicolinate
• CAS Number: 1142192-55-9
• Molecular Formula: C8H8BrNO3
• Molecular Weight: 246.058
• MDL Number: MFCD12026771
• SMILES: COC(=O)c1ncc(cc1OC)Br

Computed Properties

• Complexity: 188
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• XLogP3: 1.7

Upstream Synthesis Route

Methyl 5-bromo-3-methoxypicolinate is a versatile compound commonly employed in chemical synthesis as a key building block for the construction of various biologically active molecules. Its strategic incorporation in organic synthesis processes facilitates the introduction of functional groups and structural modifications that play a crucial role in the development of pharmaceuticals, agrochemicals, and materials science.One prominent application of Methyl 5-bromo-3-methoxypicolinate is its utilization as a precursor in the synthesis of heterocyclic compounds. The presence of the bromo and methoxy substituents on the pyridine ring enables selective functionalization reactions, allowing chemists to access a diverse array of derivatives with tailored properties. This compound serves as an essential starting material for the preparation of pyridine-based scaffolds that are prevalent in drug discovery efforts.Additionally, Methyl 5-bromo-3-methoxypicolinate is instrumental in the formation of complex molecules through cross-coupling reactions such as Suzuki-Miyaura and Heck coupling. These transformative reactions enable the formation of carbon-carbon and carbon-heteroatom bonds, thereby expanding the chemical space accessible for designing novel compounds with desired pharmacological or material characteristics.Furthermore, the unique reactivity of Methyl 5-bromo-3-methoxypicolinate makes it a valuable tool in the synthesis of natural products and analogs with potential biological activities. By leveraging the strategic placement of functional groups within the molecule, chemists can modulate the physicochemical properties and biological profiles of the synthesized compounds, driving innovation in drug design and discovery.In summary, the strategic utility of Methyl 5-bromo-3-methoxypicolinate in chemical synthesis lies in its versatile reactivity, enabling the construction of diverse molecular architectures essential for advancing various fields of science and technology.