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Structure of 76379-01-6
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This chiral building block features a protected amino group and a reactive ketone-carboxylic acid motif, enabling direct incorporation into peptide macrocycles. The tert-butoxycarbonyl group ensures stability during synthesis, while the methoxy-substituted β-ketoacid scaffold supports diverse transformations in medicinal chemistry and natural product synthesis.
(R)-2-((tert-Butoxycarbonyl)amino)-5-methoxy-5-oxopentanoic acid serves as a versatile building block for the synthesis of bioactive heterocycles and peptidomimetics. Its orthogonal functionality—comprising a protected amine, a β-keto ester motif, and a methoxy-substituted carbonyl—enables efficient cyclization and functional group interconversions under standard conditions. Bench-stable and readily purified by chromatography, it facilitates scalable access to complex scaffolds 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: