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Structure of 687-69-4
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(S)-2-(2-Aminopropanamido)acetic acid is a chiral building block featuring a protected α-amino acid scaffold with a pendant amide group. This configuration enables direct incorporation into peptide sequences without racemization, offering high fidelity in synthetic peptide assembly. The molecule exhibits enhanced solubility in aqueous and polar organic solvents, facilitating handling under standard bench conditions.
(S)-2-(2-Aminopropanamido)acetic acid serves as a chiral building block for peptide synthesis, enabling the incorporation of β-amino acid motifs with defined stereochemistry. Its amide and amino functionalities offer orthogonal reactivity for selective derivatization, while its bench-stable nature facilitates handling in standard synthetic workflows. This compound functions as a key intermediate in the construction of bioactive heterocyclic scaffolds and peptidomimetics.
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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: