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Structure of 33814-94-7
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This pyridyl-substituted amino acid derivative features a tert-butoxycarbonyl-protected amine and a carboxylic acid functionality, enabling direct incorporation into peptide synthesis. The para-pyridyl group enhances solubility and provides a handle for downstream functionalization, while the Boc protection ensures stability during reaction workflows.
2-((tert-Butoxycarbonyl)amino)-3-(pyridin-4-yl)propanoic acid serves as a versatile building block for synthesizing bioactive heterocyclic scaffolds and peptidomimetics. The protected amine and carboxylic acid functionalities enable orthogonal transformations in multistep syntheses, while the pyridin-4-yl group imparts favorable electronic and solubility properties. Bench-stable and readily purified by flash chromatography, it facilitates efficient coupling reactions and downstream deprotection protocols in medicinal chemistry workflows.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: