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Structure of 225641-86-1
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tert-Butyl N-[(1R)-3-oxocyclopentyl]carbamate features a chiral cyclopentanone-derived scaffold with a bench-stable carbamate protecting group. This configuration enables direct incorporation into asymmetric synthesis workflows, where the ketone moiety serves as a key electrophilic handle for nucleophilic addition and subsequent functionalization.
tert-Butyl N-[(1R)-3-oxocyclopentyl]carbamate serves as a stable, bench-ready chiral building block for asymmetric synthesis, enabling efficient access to functionalized cyclopentane scaffolds. The carbamate group provides orthogonal protection and facilitates selective deprotection under mild acidic conditions. Its (1R)-configured cyclopentanone moiety supports stereoselective transformations in medicinal chemistry and natural product synthesis.
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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: