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Structure of 1104083-23-9
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tert-Butyl 3-hydroxy-3-methylazetidine-1-carboxylate features a strained azetidine core bearing a hydroxyl and methyl group at the 3-position, enabling direct functionalization. The tert-butyl ester facilitates easy deprotection under mild acidic conditions. This scaffold delivers high stereocontrol in asymmetric synthesis and serves as a key building block for bioactive heterocycles.
tert-Butyl 3-hydroxy-3-methylazetidine-1-carboxylate serves as a versatile chiral building block for the synthesis of bioactive azetidine-containing scaffolds. The tertiary alcohol functionality enables straightforward functionalization via oxidation or substitution, while the protected amine facilitates sequential coupling reactions. Its bench-stable nature and compatibility with standard peptide coupling conditions make it ideal for medicinal chemistry campaigns requiring rapid access to constrained heterocycles.
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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: