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Atomfair 4,4′-Dimethyl-2,2′-bipyridine C12H12N2

Description 4,4′-Dimethyl-2,2′-bipyridine (CAS No. 1134-35-6) is a highly pure, crystalline organic compound with the molecular formula C12H12N2. This derivative of 2,2′-bipyridine features methyl groups at the 4 and 4′ positions, enhancing its electron-donating properties and making it a valuable ligand in coordination chemistry. With an IUPAC name of 4-methyl-2-(4-methylpyridin-2-yl)pyridine , it is widely utilized in catalysis, photochemistry, and materials science due to its ability to form stable complexes with transition metals. Our product is rigorously tested for purity (??98% by HPLC) and is available in convenient packaging options for laboratory and industrial use. Store in a cool, dry place, protected…

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Description

Description

4,4′-Dimethyl-2,2′-bipyridine (CAS No. 1134-35-6) is a highly pure, crystalline organic compound with the molecular formula C12H12N2. This derivative of 2,2′-bipyridine features methyl groups at the 4 and 4′ positions, enhancing its electron-donating properties and making it a valuable ligand in coordination chemistry. With an IUPAC name of 4-methyl-2-(4-methylpyridin-2-yl)pyridine, it is widely utilized in catalysis, photochemistry, and materials science due to its ability to form stable complexes with transition metals. Our product is rigorously tested for purity (??98% by HPLC) and is available in convenient packaging options for laboratory and industrial use. Store in a cool, dry place, protected from light and moisture to ensure long-term stability.

  • CAS No: 1134-35-6
  • Molecular Formula: C12H12N2
  • Molecular Weight: 184.24
  • Exact Mass: 184.100048391
  • Monoisotopic Mass: 184.100048391
  • IUPAC Name: 4-methyl-2-(4-methylpyridin-2-yl)pyridine
  • SMILES: CC1=CC(=NC=C1)C2=NC=CC(=C2)C
  • Synonyms: 1134-35-6, 4,4′-Dimethyl-2,2′-bipyridine, 2,2′-BIPYRIDINE, 4,4′-DIMETHYL-, NSC 3261, EINECS 214-483-2

Application

4,4′-Dimethyl-2,2′-bipyridine is commonly employed as a chelating ligand in transition metal catalysis, particularly in ruthenium-based photoredox catalysts for organic synthesis. It also serves as a key component in dye-sensitized solar cells (DSSCs) due to its electron-transfer properties. Researchers utilize it in supramolecular chemistry to construct metal-organic frameworks (MOFs) and other functional materials.

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