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Structure of 116437-41-3
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tert-Butyl (4-oxo-4-phenylbutyl)carbamate serves as a stable, bench-ready synthon for the introduction of a β-keto ester-like motif bearing a pendant phenyl group. This carbamate functionality enables straightforward deprotection and functionalization under mild conditions, facilitating access to complex ketone-containing architectures in synthetic and medicinal chemistry workflows.
tert-Butyl (4-oxo-4-phenylbutyl)carbamate serves as a stable, bench-friendly synthon for the introduction of a 4-oxo-4-phenylbutyl moiety in synthetic sequences. It functions as a protected precursor to β-keto amine intermediates, enabling reliable enolate formation and subsequent C–C bond construction. The carbamate group ensures good solubility and ease of purification, while the ketone functionality supports diverse transformations including reductive amination and nucleophilic addition, making it valuable in the synthesis of complex heterocycles and bioactive scaffolds.
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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: