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Structure of 183059-24-7
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tert-Butyl 2-hydroxy-2-methylpropylcarbamate features a sterically hindered carbamate group that enhances stability under standard conditions. This bench-stable derivative enables reliable protection of amine functionalities during synthetic manipulations, particularly in peptide coupling and modular synthesis workflows.
tert-Butyl 2-hydroxy-2-methylpropylcarbamate serves as a stable, bench-friendly amino protecting group precursor, enabling selective N-alkylation and subsequent deprotection under mild acidic conditions. Its tertiary butyl carbamate moiety offers excellent functional group tolerance and facilitates purification via standard chromatographic methods. The pendant hydroxyl group allows for orthogonal derivatization in complex molecule synthesis, making it a practical choice for peptide analogs and heterocyclic scaffolds requiring controlled reactivity and stability during multi-step sequences.
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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: