Description
4,4′-Dichloro-2,2′-bipyridine (CAS No. 1762-41-0) is a high-purity, halogenated bipyridine derivative with the molecular formula C10H6Cl2N2. This compound is a versatile building block in organic synthesis, particularly in the development of ligands for transition metal catalysis and coordination chemistry. Its rigid bipyridine scaffold, functionalized with chloro groups at the 4 and 4′ positions, enables precise modifications for tailored applications in materials science and pharmaceutical research. Ideal for researchers, this product is supplied with comprehensive analytical data (including 1H NMR, 13C NMR, and HPLC) to ensure quality and consistency. Store in a cool, dry place under inert conditions to maintain stability.
Properties
- CAS Number: 1762-41-0
- Complexity: 169
- IUPAC Name: 4-chloro-2-(4-chloro-2-pyridyl)pyridine
- InChI: InChI=1S/C10H6Cl2N2/c11-7-1-3-13-9(5-7)10-6-8(12)2-4-14-10/h1-6H
- InChI Key: UBSRTSGCWBPLQF-UHFFFAOYSA-N
- Exact Mass: 223.9908036
- Molecular Formula: C10H6Cl2N2
- Molecular Weight: 225.07
- SMILES: C1=CN=C(C=C1Cl)C2=NC=CC(=C2)Cl
- Topological: 25.8
- Monoisotopic Mass: 223.9908036
- Synonyms: 4,4′-Dichloro-2,2′-bipyridine, 1762-41-0, DTXSID60170096, DTXCID5092587, 2,2′-Bipyridine, 4,4′-dichloro-, 4-chloro-2-(4-chloropyridin-2-yl)pyridine, 4,4′-Dichloro-[2,2′]bipyridinyl, MFCD00233879, 4,4/’-Dichloro-2,2/’-bipyridine, SCHEMBL827247, 4,4”-Dichloro-2,2”-bipyridine, AKOS015918373, FD06271, AC-20759, AC-30729, BS-21813, SY100885, CS-0085711, 4,4 inverted exclamation mark -Dichloro-2,2 inverted exclamation mark -bipyridine
Application
4,4′-Dichloro-2,2′-bipyridine serves as a key precursor in the synthesis of functionalized bipyridine ligands for transition metal complexes, widely used in catalysis and photochemical applications. Its chloro groups facilitate further derivatization via cross-coupling reactions, making it valuable in constructing advanced materials like MOFs (Metal-Organic Frameworks) and conductive polymers. Researchers also employ it in medicinal chemistry to develop novel heterocyclic compounds with potential biological activity.
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