Atomfair 3,5-Dibromo-4-pyridinecarboxaldehyde C6H3Br2NO

Description 3,5-Dibromo-4-pyridinecarboxaldehyde (CAS No. 70201-42-2) is a high-purity brominated pyridine derivative with the molecular formula C6H3Br2NO. This compound, also known as 3,5-dibromopyridine-4-carbaldehyde, is a versatile building block in organic synthesis and pharmaceutical research. Its unique structure, featuring two bromine atoms at the 3- and 5-positions and an aldehyde group at the 4-position, makes it a valuable intermediate for cross-coupling reactions, nucleophilic substitutions, and heterocyclic scaffold construction. Suitable for researchers and scientists, this product is rigorously tested for purity and stability, ensuring reliable performance in demanding applications. Available in various quantities with detailed analytical data (HPLC, NMR, MS) upon request.

Description

3,5-Dibromo-4-pyridinecarboxaldehyde (CAS No. 70201-42-2) is a high-purity brominated pyridine derivative with the molecular formula C₆H₃Br₂NO. This compound, also known as 3,5-dibromopyridine-4-carbaldehyde, is a versatile building block in organic synthesis and pharmaceutical research. Its unique structure, featuring two bromine atoms at the 3- and 5-positions and an aldehyde group at the 4-position, makes it a valuable intermediate for cross-coupling reactions, nucleophilic substitutions, and heterocyclic scaffold construction. Suitable for researchers and scientists, this product is rigorously tested for purity and stability, ensuring reliable performance in demanding applications. Available in various quantities with detailed analytical data (HPLC, NMR, MS) upon request.

CAS No: 70201-42-2
Molecular Formula: C6H3Br2NO
Molecular Weight: 264.90
Exact Mass: 264.85609
Monoisotopic Mass: 262.85814
IUPAC Name: 3,5-dibromopyridine-4-carbaldehyde
SMILES: C1=C(C(=C(C=N1)Br)C=O)Br
Synonyms: 3,5-Dibromo-4-pyridinecarboxaldehyde, 628-673-1, 70201-42-2, 3,5-dibromoisonicotinaldehyde, 3,5-dibromopyridine-4-carbaldehyde

Application

3,5-Dibromo-4-pyridinecarboxaldehyde is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and functional materials. Its reactive aldehyde group enables condensation reactions to form Schiff bases or heterocyclic compounds, while the bromine atoms facilitate palladium-catalyzed cross-coupling (e.g., Suzuki, Heck). Researchers employ this compound in medicinal chemistry to develop kinase inhibitors and antimicrobial agents. It also serves as a precursor for luminescent materials and ligands in catalysis.

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