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Structure of 126027-07-4
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This chiral carbamate features a tert-butyl-protected amine linked to a β-keto ester moiety, enabling selective functionalization in asymmetric synthesis. The (S)-configuration ensures stereochemical fidelity during downstream transformations, while the tert-butyl group provides stability and ease of removal under mild acidic conditions.
tert-Butyl (S)-(3-oxobutan-2-yl)carbamate serves as a chiral building block for asymmetric synthesis, enabling the efficient construction of β-hydroxy and β-amino carbonyl motifs. The ketone functionality undergoes selective reduction and nucleophilic addition, while the Boc group provides orthogonal protection compatible with standard peptide coupling conditions. Its bench-stable, crystalline nature facilitates handling and purification in multi-step syntheses.
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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: