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Atomfair 3-([2,2′-Bipyridin]-4-yl)propanoic acid C13H12N2O2

Description 3-([2,2′-Bipyridin]-4-yl)propanoic acid (CAS No. 2100296-24-8) is a high-purity bipyridine derivative with the molecular formula C13H12N2O2. This compound features a propanoic acid functional group attached to the 4-position of a 2,2′-bipyridine core, making it a versatile building block for coordination chemistry, ligand synthesis, and material science applications. Its IUPAC name is 3-(2-pyridin-2-ylpyridin-4-yl)propanoic acid . The product is rigorously characterized by NMR, HPLC, and mass spectrometry to ensure ??95% purity, meeting the stringent requirements of researchers in organic synthesis, catalysis, and supramolecular chemistry. Available in milligram to gram quantities, it is supplied in sealed, light-protected vials to ensure stability.

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Description

Description

3-([2,2′-Bipyridin]-4-yl)propanoic acid (CAS No. 2100296-24-8) is a high-purity bipyridine derivative with the molecular formula C13H12N2O2. This compound features a propanoic acid functional group attached to the 4-position of a 2,2′-bipyridine core, making it a versatile building block for coordination chemistry, ligand synthesis, and material science applications. Its IUPAC name is 3-(2-pyridin-2-ylpyridin-4-yl)propanoic acid. The product is rigorously characterized by NMR, HPLC, and mass spectrometry to ensure ??95% purity, meeting the stringent requirements of researchers in organic synthesis, catalysis, and supramolecular chemistry. Available in milligram to gram quantities, it is supplied in sealed, light-protected vials to ensure stability.

  • CAS No: 2100296-24-8
  • Molecular Formula: C13H12N2O2
  • Molecular Weight: 228.25
  • Exact Mass: 228.089877630
  • Monoisotopic Mass: 228.089877630
  • IUPAC Name: 3-(2-pyridin-2-ylpyridin-4-yl)propanoic acid
  • SMILES: C1=CC=NC(=C1)C2=NC=CC(=C2)CCC(=O)O
  • Synonyms: SCHEMBL17773804, 3-([2,2′-Bipyridin]-4-yl)propanoic acid, 2100296-24-8

Application

3-([2,2′-Bipyridin]-4-yl)propanoic acid serves as a key intermediate in the synthesis of metal-organic frameworks (MOFs) and coordination polymers due to its bifunctional (carboxylate and bipyridyl) chelating properties. It is also employed in the development of luminescent probes and catalytic systems, leveraging its ability to form stable complexes with transition metals. Researchers utilize this compound in surface modification and functionalization studies for nanomaterials and biosensors.

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