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Structure of 167465-99-8
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tert-Butyl ((1S,3R)-3-hydroxycyclopentyl)carbamate is a chiral building block featuring a hydroxylated cyclopentane scaffold with defined stereochemistry. The tert-butyl carbamate group provides stable protection for primary amines, enabling controlled functionalization in complex molecule synthesis. This configuration supports efficient access to bioactive cyclic frameworks through selective derivatization and mild deprotection conditions.
tert-Butyl ((1S,3R)-3-hydroxycyclopentyl)carbamate serves as a stereochemically defined building block for cyclopentane-based scaffolds, offering bench-stable protection of primary amines with orthogonal deprotection compatibility. The pendant hydroxyl group enables selective derivatization and facilitates downstream functionalization in medicinal chemistry campaigns, particularly in the synthesis of cyclic peptide analogs and kinase inhibitors. Its predictable stereochemistry supports consistent reactivity in asymmetric synthesis workflows.
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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-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-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: