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Structure of 58160-95-5
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N-Propargylglycine features a terminal alkyne group poised for efficient bioorthogonal conjugation, enabling site-specific labeling in complex biological systems. This bench-stable amino acid derivative integrates seamlessly into peptide synthesis workflows and serves as a key building block for probing protein function through click chemistry applications.
N-Propargylglycine serves as a versatile building block in synthetic organic chemistry, enabling efficient access to bioactive heterocycles and peptidomimetics. Its propargyl group facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAC), while the α-amino acid backbone supports standard peptide coupling protocols. The compound exhibits good bench stability, ease of purification, and compatibility with diverse functional groups, making it ideal for modular library synthesis and medicinal chemistry campaigns requiring click chemistry-enabled scaffolds.
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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
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: