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Structure of 132549-43-0
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(S)-3-(tert-Butoxycarbonylamino)-5-methylhexanoic acid is a chiral building block featuring a protected amine and a carboxylic acid functional group, enabling direct incorporation into peptide synthesis. The tert-butyl carbamate moiety provides robust protection under standard conditions, while the branched alkyl chain offers steric definition for stereocontrolled coupling. This scaffold supports efficient derivatization in medicinal chemistry campaigns targeting bioactive peptides.
(S)-3-(tert-Butoxycarbonylamino)-5-methylhexanoic acid serves as a valuable chiral building block for the synthesis of peptidomimetics and bioactive heterocycles. The protected α-amino acid functions as a versatile precursor in solid-phase and solution-phase peptide coupling, offering excellent stability, straightforward deprotection under mild acidic conditions, and compatibility with diverse functional groups. Its branched aliphatic side chain enhances metabolic stability in downstream pharmaceutical scaffolds.
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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: