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Structure of 2086301-13-3
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This chiral pyrrolidine derivative features a hydroxyl group at C4 and a para-methylthiazolyl-substituted phenyl moiety, enabling precise stereochemical control in medicinal chemistry. The amide linkage and hydrochloride salt enhance solubility and stability under standard conditions, facilitating use in peptide-like scaffold synthesis and target-directed drug discovery workflows.
(2S,4R)-4-Hydroxy-N-((S)-1-(4-(4-methylthiazol-5-yl)phenyl)ethyl)pyrrolidine-2-carboxamide hydrochloride serves as a stereochemically defined building block for medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds. The molecule combines a chiral pyrrolidine core with a functionalized aryl-thiazole moiety, enabling efficient late-stage diversification via amide coupling or C–H activation. Bench-stable and readily purified by standard chromatography, it functions as a key scaffold in the synthesis of bioactive heterocycles.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: