3-Bromo-6-methoxypicolinic acid


Chemical Name: 3-Bromo-6-methoxypicolinic acid
CAS Number: 1196147-56-4
Product Number: AG000PAM(AGN-PC-0WA8B7)
Synonyms:
MDL No:
Molecular Formula: C7H6BrNO3
Molecular Weight: 232.0314

Identification/Properties


Computed Properties
Molecular Weight:
232.033g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
230.953g/mol
Monoisotopic Mass:
230.953g/mol
Topological Polar Surface Area:
59.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
176
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



3-Bromo-6-methoxypicolinic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound is particularly valued for its ability to serve as a key building block in the creation of complex organic molecules. With its unique structure, $name$ plays a crucial role in the formation of various pharmaceuticals, agrochemicals, and materials.One of the primary applications of 3-Bromo-6-methoxypicolinic acid is in the synthesis of heterocyclic compounds. Due to its bromo and methoxy functional groups, this acid serves as an excellent precursor for the construction of diverse heterocycles through organic reactions such as Suzuki coupling, Heck coupling, and palladium-catalyzed cross-coupling reactions.Furthermore, 3-Bromo-6-methoxypicolinic acid is utilized in the preparation of ligands for metal-catalyzed transformations. By incorporating this compound into ligand design, chemists can enhance the reactivity and selectivity of transition metal catalysts, leading to more efficient and sustainable synthetic processes.In addition to its role in chemical synthesis, $name$ is also employed in the development of molecular probes and imaging agents for biological studies. Its compatibility with various functionalization strategies makes it an attractive candidate for labeling biomolecules and investigating biological processes at the molecular level.Overall, 3-Bromo-6-methoxypicolinic acid is a valuable tool in the hands of synthetic chemists, enabling the construction of intricate molecular structures and facilitating the advancement of drug discovery, materials science, and chemical biology.