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Atomfair 4,7-Dimethyl-1,10-phenanthroline C14H12N2

Description 4,7-Dimethyl-1,10-phenanthroline (CAS No. 3248-05-3) is a high-purity heterocyclic compound with the molecular formula C14H12N2. This derivative of 1,10-phenanthroline features methyl groups at the 4 and 7 positions, enhancing its chelating properties and solubility in organic solvents. Widely utilized in coordination chemistry, it serves as a versatile ligand for transition metal ions, particularly in catalytic and photochemical applications. Our product is rigorously tested to ensure ??98% purity (HPLC), with trace metal analysis available upon request. Supplied as a crystalline powder, it is packaged under inert conditions to guarantee stability and longevity. Ideal for researchers in materials science, catalysis, and supramolecular…

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Description

Description

4,7-Dimethyl-1,10-phenanthroline (CAS No. 3248-05-3) is a high-purity heterocyclic compound with the molecular formula C14H12N2. This derivative of 1,10-phenanthroline features methyl groups at the 4 and 7 positions, enhancing its chelating properties and solubility in organic solvents. Widely utilized in coordination chemistry, it serves as a versatile ligand for transition metal ions, particularly in catalytic and photochemical applications. Our product is rigorously tested to ensure ??98% purity (HPLC), with trace metal analysis available upon request. Supplied as a crystalline powder, it is packaged under inert conditions to guarantee stability and longevity. Ideal for researchers in materials science, catalysis, and supramolecular chemistry.

  • CAS No: 3248-05-3
  • Molecular Formula: C14H12N2
  • Molecular Weight: 208.26
  • Exact Mass: 208.100048391
  • Monoisotopic Mass: 208.100048391
  • IUPAC Name: 4,7-dimethyl-1,10-phenanthroline
  • SMILES: CC1=C2C=CC3=C(C=CN=C3C2=NC=C1)C
  • Synonyms: 4,7-Dimethyl-1,10-phenanthroline, 3248-05-3, 1,10-Phenanthroline, 4,7-dimethyl-, 4,7-Dimethyl-o-phenanthroline, 4,7-DIMETHYL-[1,10]PHENANTHROLINE

Application

4,7-Dimethyl-1,10-phenanthroline is primarily employed as a chelating ligand for copper(I) in catalytic systems, including click chemistry and atom transfer radical polymerization (ATRP). Its sterically hindered structure improves selectivity in metal-ion recognition, making it valuable in sensor development. The compound also finds use in photophysical studies due to its ability to form luminescent complexes with lanthanides and transition metals.

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