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Structure of 56502-01-3
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(S)-2-(1-Boc-2-pyrrolidinyl)acetic acid features a chiral pyrrolidine core with a stable Boc-protected amine, enabling direct incorporation into peptide syntheses and asymmetric catalysis. The carboxylic acid moiety facilitates coupling reactions under standard conditions, while the sterically hindered pyrrolidine ring enhances conformational control in bioactive molecule design.
(S)-2-(1-Boc-2-pyrrolidinyl)acetic acid serves as a versatile chiral building block for the synthesis of bioactive molecules, particularly in medicinal chemistry and peptide conjugation. The Boc-protected pyrrolidine moiety offers excellent bench stability and orthogonal deprotection compatibility, while the pendant carboxylic acid enables facile coupling reactions. This structure facilitates access to constrained peptidomimetics and heterocyclic scaffolds commonly found in drug discovery programs.
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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-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: