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*For research and further manufacturing use only, not for direct human use.
Structure of 141850-54-6
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This chiral pyrrolidine derivative features a bench-stable tert-butyl ester and hydroxymethyl functionality, enabling direct incorporation into complex molecular architectures. The (2R,4R) stereochemistry ensures high diastereoselectivity in downstream transformations, while the protected alcohol groups offer orthogonal reactivity for selective derivatization under mild conditions.
(2R,4R)-tert-Butyl 4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate serves as a versatile chiral building block in medicinal chemistry, enabling efficient access to pyrrolidine-containing scaffolds. The molecule features two orthogonal hydroxyl groups and a stable tert-butyl carbamate protecting group, facilitating selective derivatization and downstream functionalization. Its bench-stable nature and compatibility with standard coupling and reduction protocols make it ideal for multi-step synthesis of bioactive molecules.
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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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: