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Atomfair 3-Methyl-2-phenylpyridine C12H11N
Description 3-Methyl-2-phenylpyridine (CAS No. 10273-90-2) is a high-purity heterocyclic organic compound with the molecular formula C12H11N . This specialized chemical features a pyridine ring substituted with a methyl group at the 3-position and a phenyl group at the 2-position, offering unique electronic and steric properties for advanced research applications. Available in various quantities with ??98% purity (HPLC/GC), it is ideal for pharmaceutical intermediates, ligand synthesis, and material science research. The compound is supplied in sealed, light-resistant containers under inert gas to ensure stability. Technical data including1H/13C NMR spectra, mass spectrometry, and HPLC chromatograms are available upon request. Store at 2-8??C…
Description
Description
3-Methyl-2-phenylpyridine (CAS No. 10273-90-2) is a high-purity heterocyclic organic compound with the molecular formula C12H11N. This specialized chemical features a pyridine ring substituted with a methyl group at the 3-position and a phenyl group at the 2-position, offering unique electronic and steric properties for advanced research applications. Available in various quantities with ??98% purity (HPLC/GC), it is ideal for pharmaceutical intermediates, ligand synthesis, and material science research. The compound is supplied in sealed, light-resistant containers under inert gas to ensure stability. Technical data including 1H/13C NMR spectra, mass spectrometry, and HPLC chromatograms are available upon request. Store at 2-8??C in a dry environment.
- CAS No: 10273-90-2
- Molecular Formula: C12H11N
- Molecular Weight: 169.22
- Exact Mass: 169.089149355
- Monoisotopic Mass: 169.089149355
- IUPAC Name: 3-methyl-2-phenylpyridine
- SMILES: CC1=C(N=CC=C1)C2=CC=CC=C2
- Synonyms: 3-Methyl-2-phenylpyridine, 10273-90-2, Pyridine, 3-methyl-2-phenyl-, 3-Picoline, 2-phenyl-, OIY9I0GL3Z
Application
3-Methyl-2-phenylpyridine serves as a key building block in medicinal chemistry for developing kinase inhibitors and CNS-active compounds. Its sterically hindered pyridine core facilitates chelation in transition metal catalyst systems for cross-coupling reactions. Researchers utilize this compound in OLED material development due to its electron-transporting characteristics and thermal stability.
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