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Structure of 72597-18-3
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(R)-Benzyl 2-(hydroxymethyl)pyrrolidine-1-carboxylate features a chiral pyrrolidine scaffold with a pendant hydroxymethyl group, enabling direct functionalization in asymmetric synthesis. This bench-stable derivative integrates readily into cascade reactions and serves as a key building block for bioactive alkaloid frameworks.
(R)-Benzyl 2-(hydroxymethyl)pyrrolidine-1-carboxylate serves as a versatile chiral building block for the synthesis of pyrrolidine-containing pharmaceuticals and bioactive molecules. The hydroxymethyl group enables straightforward functionalization via oxidation, protection, or coupling reactions, while the benzyl ester offers convenient deprotection under mild hydrogenolysis conditions. Its stereochemical purity supports high diastereoselectivity in downstream transformations, making it ideal for medicinal chemistry applications requiring defined stereocenters.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2810
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H319
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Precautionary Statements : P264-P270-P280-P330-P405-P501
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Lot numbers can be found on the outside label of a product: