Description
2-(Pyridin-2-yl)aniline (CAS No. 29528-30-1) is a high-purity organic compound with the molecular formula C11H10N2, widely utilized in pharmaceutical research, coordination chemistry, and material science. This compound features a pyridine ring ortho-substituted with an aniline group, making it a versatile building block for synthesizing heterocyclic compounds, ligands, and catalysts. Its unique structure enables chelation with transition metals, facilitating applications in catalysis and supramolecular chemistry. Available in various quantities, our product undergoes rigorous QC testing (including HPLC, NMR, and MS) to ensure ≥98% purity, meeting the stringent demands of academic and industrial researchers. Proper storage under inert conditions is recommended to maintain stability.
Properties
- CAS Number: 29528-30-1
- Complexity: 158
- IUPAC Name: 2-(2-pyridyl)aniline
- InChI: InChI=1S/C11H10N2/c12-10-6-2-1-5-9(10)11-7-3-4-8-13-11/h1-8H,12H2
- InChI Key: VPZCNNNHCMBJCM-UHFFFAOYSA-N
- Exact Mass: 170.084398327
- Molecular Formula: C11H10N2
- Molecular Weight: 170.21
- SMILES: C1=CC=C(C(=C1)C2=CC=CC=N2)N
- Topological: 38.9
- Monoisotopic Mass: 170.084398327
- Synonyms: 2-(pyridin-2-yl)aniline, 29528-30-1, 2-(2-Pyridyl)aniline, 2-pyridin-2-ylaniline, 2-Pyridin-2-yl-phenylamine, benzenamine, 2-(2-pyridinyl)-, 2-(2-Pyridinyl)Benzenamine, MFCD03426328, (aminophenyl)pyridine, 2-(2-Pyridinyl)aniline, ortho-(2-pyridyl)aniline, 2-(o-Aminophenyl)pyridine, 2-(2-Aminophenyl)pyridine, SCHEMBL819951, SCHEMBL4055597, SCHEMBL4976600, SCHEMBL9207301, DTXSID90952024, VPZCNNNHCMBJCM-UHFFFAOYSA-N, BCP32482, AKOS012990188, AB14825, BS-22243, DB-068133, CS-0213295, N12890, P24941, 2-(2-Pyridyl)aniline;2-(2-Aminophenyl)pyridine;2-(2-pyridinyl)Benzenamine, InChI=1/C11H10N2/c12-10-6-2-1-5-9(10)11-7-3-4-8-13-11/h1-8H,12H, 6048-22-2
Application
2-(Pyridin-2-yl)aniline serves as a key intermediate in the synthesis of nitrogen-containing heterocycles and metal-organic frameworks (MOFs). It is employed in the development of luminescent materials and as a ligand for transition-metal catalysts in cross-coupling reactions. Researchers also utilize it to study charge-transfer complexes and as a precursor for bioactive molecules in medicinal chemistry.
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