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Structure of 847416-99-3
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tert-Butyl (3-oxocyclopentyl)carbamate features a cyclopentanone ring tethered to a carbamate group, enabling direct incorporation into complex molecular architectures. This stable, moisture-tolerant reagent facilitates efficient synthesis of functionalized cyclopentane derivatives under standard conditions.
tert-Butyl (3-oxocyclopentyl)carbamate serves as a versatile synthon in synthetic organic chemistry, enabling efficient access to functionalized cyclopentane scaffolds. The protected amine and ketone functionalities offer orthogonal reactivity for downstream transformations, including selective reductions, nucleophilic additions, and transition-metal-catalyzed couplings. Its bench-stable nature and ease of purification make it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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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: