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Structure of 632352-56-8
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tert-Butyl 4-oxo-3-phenylpiperidine-1-carboxylate features a sterically hindered tert-butyl ester and a conjugated ketone, enabling direct functionalization at the C4 position. The phenyl group enhances π-stacking potential in molecular scaffolds, while the bench-stable carbamate facilitates modular synthesis of bioactive piperidines under standard conditions.
tert-Butyl 4-oxo-3-phenylpiperidine-1-carboxylate serves as a versatile scaffold for the synthesis of biologically relevant piperidine derivatives. The ketone functionality enables enolate formation and nucleophilic addition, while the tert-butoxycarbonyl group offers convenient protection and orthogonal deprotection. Its stability under standard reaction conditions facilitates functionalization at C4 and C3 positions, supporting applications in medicinal chemistry and heterocycle construction.
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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: