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Structure of 167216-22-0
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This Boc-protected amino alcohol features a tertiary hydroxyl group flanked by a methyl substituent, enabling selective derivatization in peptide synthesis. The stable Boc moiety permits straightforward deprotection under mild acidic conditions, while the sterically hindered backbone resists racemization during coupling steps.
3-(Boc-amino)-3-methyl-1-butanol serves as a versatile amino alcohol building block for peptide and heterocyclic synthesis. The Boc-protected amine enables orthogonal functional group manipulation, while the primary alcohol facilitates coupling reactions or derivatization. Its tertiary alcohol structure provides enhanced bench stability and simplifies purification. This compound functions effectively in standard amide coupling protocols and supports the construction of complex scaffolds in 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: