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Structure of 84348-37-8
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N-Boc-4-oxo-L-proline features a protected amine and a ketone-functionalized pyrrolidine ring, enabling direct incorporation into peptide syntheses. This bench-stable derivative supports efficient access to oxoprolines in bioactive molecule development.
N-Boc-4-oxo-L-proline serves as a versatile building block in peptide synthesis and heterocyclic chemistry, enabling efficient access to pyrrolidine-based scaffolds. The Boc group provides excellent stability and ease of removal under mild acidic conditions, while the 4-oxo functionality supports diverse transformations including reductive amination and nucleophilic addition. Its compatibility with standard coupling protocols and predictable reactivity make it a reliable choice for constructing complex bioactive molecules.
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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-H319
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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: