Description

5-Bromo-2,4-dimethylpyridine (CAS No. 27063-92-9) is a high-purity brominated pyridine derivative with the molecular formula C₇H₈BrN. This heterocyclic organic compound is characterized by its two methyl groups at the 2- and 4-positions and a bromine substituent at the 5-position of the pyridine ring. It is a valuable intermediate in pharmaceutical, agrochemical, and materials science research, offering versatile reactivity for cross-coupling reactions, nucleophilic substitutions, and metal-catalyzed transformations. Available in >98% purity (HPLC), this compound is supplied in rigorously tested batches to ensure consistency for synthetic applications. Proper handling under inert conditions is recommended due to its sensitivity to moisture and air.

Properties

• CAS Number: 27063-92-9
• Complexity: 94.9
• IUPAC Name: 5-bromo-2,4-dimethyl-pyridine
• InChI: InChI=1S/C7H8BrN/c1-5-3-6(2)9-4-7(5)8/h3-4H,1-2H3
• InChI Key: SLMUXUHXAIPROA-UHFFFAOYSA-N
• Exact Mass: 184.98401
• Molecular Formula: C7H8BrN
• Molecular Weight: 186.05
• SMILES: CC1=CC(=NC=C1Br)C
• Topological: 12.9
• Monoisotopic Mass: 184.98401
• Synonyms: 5-Bromo-2,4-dimethylpyridine, 27063-92-9, MFCD09842454, PYRIDINE, 5-BROMO-2,4-DIMETHYL-, SCHEMBL2875605, SCHEMBL28811811, DTXSID80539929, SLMUXUHXAIPROA-UHFFFAOYSA-N, AKOS006310450, 5-Bromo-2 pound not4-dimethylpyridine, AB53714, CS-W022304, AC-27074, AS-59352, SY102457, DB-082560, EN300-108803, W18180

Application

5-Bromo-2,4-dimethylpyridine serves as a key building block in medicinal chemistry for the synthesis of bioactive molecules, particularly kinase inhibitors and antiviral agents. Its bromine moiety enables efficient Suzuki-Miyaura and Buchwald-Hartwig couplings for drug discovery pipelines. The compound is also employed in ligand design for catalytic systems and as a precursor for functionalized pyridine-based materials in optoelectronics.

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