Description

(6-Aminopyridin-2-yl)(1-methylpiperidin-4-yl)methanone (CAS No. 613678-03-8) is a high-purity organic compound with the molecular formula C₁₂H₁₇N₃O. This specialized chemical features a unique structural motif combining a 6-aminopyridine moiety with a 1-methylpiperidin-4-yl ketone group, making it a valuable intermediate for pharmaceutical research and medicinal chemistry applications. The compound is supplied as a solid with ≥95% purity (HPLC) and is rigorously tested for quality assurance. Proper storage conditions (2-8°C, under inert atmosphere) are recommended to maintain stability. Available in research quantities from 100mg to 10g, with custom synthesis options available for bulk requirements.

Properties

• CAS Number: 613678-03-8
• Complexity: 249
• IUPAC Name: (6-amino-2-pyridyl)-(1-methyl-4-piperidyl)methanone
• InChI: InChI=1S/C12H17N3O/c1-15-7-5-9(6-8-15)12(16)10-3-2-4-11(13)14-10/h2-4,9H,5-8H2,1H3,(H2,13,14)
• InChI Key: YLTJVIIEHKBRPA-UHFFFAOYSA-N
• Exact Mass: 219.137162174
• Molecular Formula: C12H17N3O
• Molecular Weight: 219.28
• SMILES: CN1CCC(CC1)C(=O)C2=NC(=CC=C2)N
• Topological: 59.2
• Monoisotopic Mass: 219.137162174
• Synonyms: (6-Aminopyridin-2-yl)(1-methylpiperidin-4-yl)methanone, 613678-03-8, DTXSID20464746, DTXCID10415565, (6-aminopyridin-2-yl)-(1-methylpiperidin-4-yl)methanone, MFCD22575148, 2-Amino-6-(1-methylpiperidin-4-ylcarbonyl)pyridine, (6-Amino-2-pyridinyl)(1-methyl-4-piperidinyl)methanone, Methanone, (6-amino-2-pyridinyl)(1-methyl-4-piperidinyl)-, 6-(1-METHYLPIPERIDINE-4-CARBONYL)PYRIDIN-2-AMINE, L3EX9544DY, SCHEMBL2533687, YLTJVIIEHKBRPA-UHFFFAOYSA-N, BCP17048, SB73984, BS-49738, SY274040, DB-344795, CS-0021415, E84260, (6-Amino-2-pyridyl)(1-methyl-4-piperidyl)methanone

Application

This compound serves as a key building block in the synthesis of novel pharmaceutical candidates, particularly in CNS-targeting drug discovery. Researchers utilize its structural features for developing potential kinase inhibitors and neurotransmitter modulators. The molecule’s dual functionality makes it valuable for structure-activity relationship studies in medicinal chemistry programs.

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