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Atomfair 3-Bromo-5-methylpyridine-2-carboxylic acid C7H6BrNO2
Description 3-Bromo-5-methylpyridine-2-carboxylic acid (CAS No. 1211515-68-2) is a high-purity heterocyclic carboxylic acid derivative with the molecular formula C7H6BrNO2. This compound features a pyridine core substituted with a bromine atom at the 3-position, a methyl group at the 5-position, and a carboxylic acid moiety at the 2-position, making it a versatile building block for pharmaceutical and agrochemical synthesis. With a molecular weight of 216.03 g/mol, it is supplied as a fine white to off-white crystalline powder, ensuring optimal solubility in polar organic solvents. Ideal for researchers and industrial chemists, this product is rigorously tested via HPLC, NMR, and mass spectrometry to…
Description
Description
3-Bromo-5-methylpyridine-2-carboxylic acid (CAS No. 1211515-68-2) is a high-purity heterocyclic carboxylic acid derivative with the molecular formula C7H6BrNO2. This compound features a pyridine core substituted with a bromine atom at the 3-position, a methyl group at the 5-position, and a carboxylic acid moiety at the 2-position, making it a versatile building block for pharmaceutical and agrochemical synthesis. With a molecular weight of 216.03 g/mol, it is supplied as a fine white to off-white crystalline powder, ensuring optimal solubility in polar organic solvents. Ideal for researchers and industrial chemists, this product is rigorously tested via HPLC, NMR, and mass spectrometry to guarantee ??98% purity. Suitable for use in cross-coupling reactions, metal-catalyzed transformations, and as a precursor for bioactive molecule development.
- CAS No: 1211515-68-2
- Molecular Formula: C7H6BrNO2
- Molecular Weight: 216.03
- Exact Mass: 214.95819
- Monoisotopic Mass: 214.95819
- IUPAC Name: 3-bromo-5-methylpyridine-2-carboxylic acid
- SMILES: CC1=CC(=C(N=C1)C(=O)O)Br
- Synonyms: 1211515-68-2, 3-Bromo-5-methylpyridine-2-carboxylic acid, DTXSID50694175, DTXCID60644924, 695-972-1
Application
3-Bromo-5-methylpyridine-2-carboxylic acid serves as a key intermediate in the synthesis of pharmaceuticals, particularly for the development of kinase inhibitors and antiviral agents. Its reactive bromine and carboxylic acid groups enable facile derivatization for drug discovery pipelines. This compound is also employed in material science for constructing functionalized pyridine-based ligands in catalysis. Researchers utilize it in Suzuki-Miyaura and Buchwald-Hartwig coupling reactions to access complex heterocyclic architectures.
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