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Structure of 167298-40-0
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tert-Butyl N-[(1S)-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 reactive handle for stereoselective transformations and downstream functionalization.
tert-Butyl N-[(1S)-3-oxocyclopentyl]carbamate serves as a stable, bench-ready chiral building block featuring a masked amine and a cyclopentanone moiety. It enables stereoselective functionalization at the C3 position and facilitates efficient access to substituted cyclopentane scaffolds via reductive cleavage or directed transformations. Its compatibility with standard coupling and protection protocols makes it ideal for iterative synthesis in medicinal chemistry and natural product derivatization.
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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: