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Structure of 1035351-06-4
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This azetidine derivative features a tert-butoxycarbonyl-protected amine and a hydroxyl group on the ring, enabling direct incorporation into peptide synthesis. The protected amine facilitates selective functionalization, while the hydroxy group provides a handle for further derivatization or conjugation under standard conditions.
1-[(Tert-butoxy)carbonyl]-3-hydroxyazetidine-3-carboxylic acid serves as a versatile building block for the synthesis of azetidinone-containing scaffolds and bioactive heterocycles. The protected hydroxyl and carboxylic acid functionalities enable orthogonal transformations, while the strained azetidine ring facilitates nucleophilic ring-opening reactions. Its bench-stable tert-butyl carbamate group simplifies purification and allows sequential functionalization in multi-step syntheses.
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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: