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Structure of 613678-03-8
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This pyridine-piperidine hybrid delivers a strategically positioned amine and carbonyl for targeted conjugation. The 6-amino-2-pyridinyl moiety enables metal coordination and hydrogen bonding, while the 1-methyl-4-piperidinyl group provides solubility and steric resilience. Bench-stable under standard conditions, it integrates readily into medicinal chemistry scaffolds requiring polar, nitrogen-rich motifs.
(6-Amino-2-pyridinyl)(1-methyl-4-piperidinyl)methanone serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through amide coupling and cyclization reactions. Its pyridine-amino motif offers enhanced solubility and hydrogen-bonding capacity, while the piperidinyl carbonyl functions as a stable, synthetically accessible handle for further derivatization. The compound exhibits good bench stability and facilitates purification via standard chromatographic methods, making it well-suited for iterative synthesis campaigns in API development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: