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Structure of 885102-34-1
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tert-Butyl 3-methyl-4-oxopyrrolidine-1-carboxylate features a sterically hindered pyrrolidine core with a ketone at C4 and a methyl group at C3, enabling selective functionalization. The tert-butyl carbamate moiety offers stability and convenient deprotection under mild acidic conditions, making it valuable for peptide backbone modifications and heterocyclic synthesis.
tert-Butyl 3-methyl-4-oxopyrrolidine-1-carboxylate serves as a stable, bench-ready building block for the synthesis of pyrrolidine-based scaffolds. Its 4-oxo functionality enables efficient enolization and nucleophilic addition, while the tert-butoxycarbonyl group provides orthogonal protection compatible with standard amine deprotection protocols. The methyl substitution enhances stereochemical control in subsequent transformations, facilitating access to diverse heterocyclic frameworks relevant to medicinal chemistry and process development.
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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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: