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Structure of 87205-47-8
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(R)-2-Aminopent-4-ynoic acid hydrochloride features a chiral α-amino acid scaffold with a terminal alkyne handle, enabling bioorthogonal conjugation in peptide and probe synthesis. The hydrochloride salt enhances solubility and stability under standard bench conditions, facilitating straightforward handling in aqueous and organic media. This derivative integrates efficiently into diverse molecular architectures through click chemistry or amide coupling protocols.
(R)-2-Aminopent-4-ynoic acid hydrochloride serves as a versatile building block for the synthesis of bioactive heterocycles and peptidomimetics. Its terminal alkyne and α-amino carboxylic acid functionalities enable efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC) and direct incorporation into peptide chains. The hydrochloride salt enhances bench stability and simplifies handling, while the stereochemically defined (R)-configuration ensures predictable reactivity in asymmetric synthesis.
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: