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Structure of 1539946-20-7
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tert-Butyl 2-methyl-3-oxopyrrolidine-1-carboxylate features a sterically hindered pyrrolidinone core with a bench-stable tert-butyl ester, enabling direct incorporation into complex molecular architectures. The carbonyl group at C3 enhances electrophilicity for nucleophilic addition, while the methyl substituent provides controlled steric profile. This building block streamlines access to chiral amine scaffolds in medicinal chemistry and peptide conjugation workflows.
tert-Butyl 2-methyl-3-oxopyrrolidine-1-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to pyrrolidine-containing scaffolds. The ketone functionality at C3 facilitates nucleophilic addition and reductive amination reactions, while the tert-butoxycarbonyl (Boc) group provides stable protection for nitrogen. Its bench-stable nature and compatibility with a broad range of reaction conditions make it ideal for iterative synthesis and fragment assembly 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: