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Structure of 192214-05-4
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(R)-Benzyl 3-(hydroxymethyl)pyrrolidine-1-carboxylate features a chiral pyrrolidine core with a pendant hydroxymethyl group, enabling selective functionalization in asymmetric synthesis. This bench-stable intermediate integrates readily into medicinal chemistry campaigns requiring stereocontrolled access to nitrogen-containing scaffolds.
(R)-Benzyl 3-(hydroxymethyl)pyrrolidine-1-carboxylate serves as a versatile chiral building block in medicinal chemistry, enabling efficient access to pyrrolidine-containing scaffolds. The hydroxymethyl group facilitates downstream functionalization via oxidation, protection, or coupling reactions, while the benzyl ester provides stability and ease of removal under standard hydrogenolysis conditions. Its stereochemical integrity supports reliable asymmetric synthesis workflows.
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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: