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Structure of 1903-75-9
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N-Methylpiperidine-4-carboxamide hydrochloride features a rigid, electron-rich piperidine core paired with a polar amide functionality, enabling strong hydrogen bonding and enhanced solubility in aqueous and protic solvents. This combination supports efficient incorporation into bioactive molecules, particularly in kinase inhibitors and CNS-targeted therapeutics, where metabolic stability and membrane permeability are critical. The hydrochloride salt form ensures improved crystallinity and handling under standard bench conditions.
N-Methylpiperidine-4-carboxamide hydrochloride serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive scaffolds through standard amide coupling and reductive amination protocols. Its stability under routine synthetic conditions, combined with favorable solubility and ease of purification, facilitates integration into high-throughput synthesis workflows. Functions effectively as a key intermediate in the construction of heterocyclic pharmacophores and peptide-like motifs.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: