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Atomfair 6-Chloro-2-iodo-3-methoxypyridine C6H5ClINO
Description 6-Chloro-2-iodo-3-methoxypyridine (CAS No. 1256790-05-2) is a high-purity halogenated pyridine derivative with the molecular formula C6H5ClINO . This compound is a valuable heterocyclic building block for pharmaceutical and agrochemical research, featuring both chloro and iodo substituents on a methoxy-functionalized pyridine ring. Its unique structure enables versatile reactivity in cross-coupling reactions (e.g., Suzuki, Stille) , nucleophilic substitutions, and metal-catalyzed transformations. Supplied as a crystalline solid with ??95% purity (HPLC), it is rigorously tested by GC/MS, NMR, and elemental analysis to ensure batch-to-batch consistency. Ideal for medicinal chemistry applications, this intermediate is packaged under inert gas in amber glass vials to ensure…
Description
Description
6-Chloro-2-iodo-3-methoxypyridine (CAS No. 1256790-05-2) is a high-purity halogenated pyridine derivative with the molecular formula C6H5ClINO. This compound is a valuable heterocyclic building block for pharmaceutical and agrochemical research, featuring both chloro and iodo substituents on a methoxy-functionalized pyridine ring. Its unique structure enables versatile reactivity in cross-coupling reactions (e.g., Suzuki, Stille), nucleophilic substitutions, and metal-catalyzed transformations. Supplied as a crystalline solid with ??95% purity (HPLC), it is rigorously tested by GC/MS, NMR, and elemental analysis to ensure batch-to-batch consistency. Ideal for medicinal chemistry applications, this intermediate is packaged under inert gas in amber glass vials to ensure stability. Synonyms include DTXSID10857320 and DTXCID80808061.
- CAS No: 1256790-05-2
- Molecular Formula: C6H5ClINO
- Molecular Weight: 269.47
- Exact Mass: 268.91044
- Monoisotopic Mass: 268.91044
- IUPAC Name: 6-chloro-2-iodo-3-methoxypyridine
- SMILES: COC1=C(N=C(C=C1)Cl)I
- Synonyms: 6-CHLORO-2-IODO-3-METHOXYPYRIDINE, 1256790-05-2, DTXSID10857320, DTXCID80808061, 102-880-2
Application
6-Chloro-2-iodo-3-methoxypyridine serves as a key intermediate in the synthesis of biologically active molecules, particularly in drug discovery for kinase inhibitors and CNS-targeting compounds. Its iodo substituent facilitates palladium-catalyzed cross-coupling reactions to construct complex heteroaromatic scaffolds. Researchers utilize this compound in structure-activity relationship (SAR) studies due to its dual halogen functionality, enabling selective derivatization. It is also employed in the development of agrochemicals and fluorescent probes.
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