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Structure of 66659-20-9
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This hydrochloride salt features a 2-aminothiazol-4-yl moiety linked to an acetic acid side chain, delivering enhanced solubility and stability under standard conditions. The scaffold integrates readily into peptide-based conjugates and bioactive molecules, serving as a robust building block for medicinal chemistry campaigns targeting kinase inhibition and antimicrobial agents.
2-(2-Aminothiazol-4-yl)acetic acid hydrochloride serves as a key building block for thiazole-containing pharmaceuticals, enabling efficient access to bioactive scaffolds through standard amide coupling and electrophilic substitution reactions. Its amine functionality offers high reactivity in peptide synthesis and derivatization workflows, while the hydrochloride salt enhances solubility and bench stability. Functions reliably in diverse synthetic contexts requiring nitrogen heterocycles with orthogonal functional handles.
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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: