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Structure of 368866-33-5
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This chiral building block features a tert-butyl carbamate-protected amino group and a pendant oxan-4-yl side chain, enabling direct incorporation into peptide syntheses. The sterically hindered tert-butyl carbonyl moiety ensures stability during handling and reaction workflows.
(2S)-2-[(2-Methylpropan-2-yl)oxycarbonylamino]-3-(oxan-4-yl)propanoic acid serves as a versatile chiral building block for peptide and heterocyclic synthesis, leveraging its protected α-amino acid scaffold. The tert-butoxycarbonyl (Boc) group enables stable storage and straightforward deprotection under mild acidic conditions, while the oxan-4-yl moiety provides a rigid, polar substituent suitable for modulating solubility and conformational preference in medicinal chemistry applications. This compound exhibits excellent functional group tolerance and facilitates efficient coupling reactions in standard solid-phase and solution-phase 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 : 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: