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Structure of 630421-46-4
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This chiral pyrrolidine derivative features a protected amino acid moiety and hydroxyl group, enabling direct incorporation into peptide-based scaffolds. The (2S,4R) stereochemistry ensures high diastereoselectivity in coupling reactions, while the tert-butoxycarbonyl group provides stability under standard bench conditions.
(2S,4R)-1-((S)-2-((tert-butoxycarbonyl)amino)-3,3-dimethylbutanoyl)-4-hydroxypyrrolidine-2-carboxylic acid serves as a versatile chiral building block for the synthesis of peptidomimetics and bioactive heterocycles. The hydroxyl group enables selective derivatization, while the Boc-protected amine and carboxylic acid facilitate orthogonal functionalization. Its stability under standard reaction conditions and compatibility with common coupling protocols make it ideal for modular peptide and macrocycle assembly in medicinal chemistry workflows.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: