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Structure of 661458-35-1
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1-(tert-Butoxycarbonyl)-4-oxopiperidine-2-carboxylic acid features a protected piperidine scaffold with orthogonal functionality, enabling direct incorporation into peptide synthesis. The ketone and carboxylic acid moieties offer complementary reactivity for late-stage diversification. This bench-stable derivative facilitates efficient access to bioactive cyclic scaffolds in medicinal chemistry campaigns.
1-(tert-Butoxycarbonyl)-4-oxopiperidine-2-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of piperidine-based scaffolds prevalent in bioactive molecules. The protected amine and keto-carboxylic acid functionalities offer orthogonal reactivity for peptide coupling and selective reductions, while the tert-butyl carbamate group ensures stability during storage and standard synthetic manipulations. Its bench-stable nature and compatibility with common purification methods facilitate efficient route design for drug discovery campaigns.
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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: