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Structure of 32404-28-7
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This chiral amino acid derivative features a phenolic hydroxyl group and a ketone-bearing aromatic ring, enabling selective conjugation in bioconjugation workflows. The hydrochloride salt enhances solubility and stability under standard conditions, facilitating handling in synthetic peptide assembly and medicinal chemistry applications.
(S)-3-(3-Acetyl-4-hydroxyphenyl)-2-aminopropanoic acid hydrochloride serves as a key chiral building block for bioactive phenolic amino acids, enabling access to diverse heterocyclic scaffolds via standard peptide coupling and cyclization protocols. Its bench-stable hydrochloride salt facilitates handling and purification, while the acetyl and phenolic functionalities support orthogonal derivatization in medicinal chemistry campaigns.
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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: