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Structure of 1009335-39-0
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This chiral pyrrolidine derivative features a phenyl group at the 2-position and hydroxymethyl functionality at C4, enabling direct integration into complex molecular architectures. The stereochemistry at C2 and C4 ensures high diastereoselectivity in downstream transformations, while the hydroxyl and carboxylate moieties provide orthogonal handles for selective derivatization. This scaffold serves as a robust building block in medicinal chemistry and asymmetric synthesis workflows.
(2R,4R)-Phenyl-4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate serves as a stereochemically defined pyrrolidine scaffold for medicinal chemistry and natural product synthesis. Its orthogonal hydroxyl and carboxylate functionalities enable selective derivatization, while the chiral centers provide access to enantioselective transformations. The compound exhibits bench stability and facilitates efficient purification, making it suitable for multi-step syntheses and API intermediate 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
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Lot numbers can be found on the outside label of a product: