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Structure of 1208087-83-5
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This piperidine-based scaffold integrates a 2-chloropyrimidin-4-yl group, delivering enhanced electrophilic reactivity and metabolic stability. The carboxylic acid functionality enables direct conjugation or salt formation, supporting efficient derivatization in medicinal chemistry campaigns. Designed for robust performance under standard bench conditions.
1-(2-Chloropyrimidin-4-yl)piperidine-4-carboxylic acid serves as a versatile building block for the synthesis of bioactive heterocycles, particularly in medicinal chemistry and agrochemical research. The molecule combines a reactive 2-chloropyrimidine moiety with a piperidine carboxylic acid scaffold, enabling efficient coupling reactions via nucleophilic substitution or amide formation. Its bench-stable nature, predictable reactivity, and compatibility with standard purification methods make it well-suited for modular synthesis workflows.
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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-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: