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Structure of 149632-73-5
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tert-Butyl (1-aminopropan-2-yl)carbamate delivers a protected serine surrogate with enhanced stability and solubility in organic media. This bench-stable carbamate incorporates a chiral β-amino alcohol scaffold, enabling direct incorporation into peptide sequences or as a building block for bioactive small molecules. The tert-butyl group facilitates convenient deprotection under mild acidic conditions, streamlining synthetic workflows.
tert-Butyl (1-aminopropan-2-yl)carbamate serves as a stable, bench-friendly amino protecting group derivative, enabling selective N-alkylation and amide bond formation under standard conditions. Its tert-butyl carbamate moiety offers orthogonal deprotection compatibility with acid-labile functionalities, facilitating efficient synthesis of complex intermediates in peptide and 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 : 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: