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Structure of 201594-84-5
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This chiral pyridine derivative features a piperidinyl ether linkage and a 4-chlorophenyl substituent, delivering enhanced metabolic stability and targeted bioavailability. The (S)-stereoisomer enables precise pharmacophore alignment in CNS-directed small molecule development.
(S)-2-((4-Chlorophenyl)(piperidin-4-yloxy)methyl)pyridine serves as a versatile building block in medicinal chemistry, enabling the construction of complex heterocyclic scaffolds. Its well-defined stereochemistry and stable functional groups—particularly the pyridine, piperidinyl ether, and chlorophenyl moieties—facilitate predictable reactivity in coupling reactions and downstream modifications. The molecule exhibits robust bench stability and is amenable to standard purification techniques, making it suitable for high-throughput synthesis and process development workflows.
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GHS No : GHS07,GHS05
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Signal Word : Danger
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UN#: 2735
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P310-P312-P330-P332+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: