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Structure of 389890-43-1
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tert-Butyl (cis-3-hydroxycyclobutyl)carbamate features a stereochemically defined cyclobutane scaffold with a hydroxyl group in the cis configuration, offering enhanced stability and predictable reactivity. This bench-stable carbamate derivative facilitates efficient incorporation into complex molecular architectures, particularly in medicinal chemistry campaigns requiring constrained ring systems. The protecting group enables selective deprotection under mild conditions, streamlining synthetic sequences involving sensitive intermediates.
tert-Butyl (cis-3-hydroxycyclobutyl)carbamate serves as a stable, bench-friendly building block for cyclobutane-containing scaffolds. The cis-configured hydroxyl group enables selective functionalization and acts as a handle for derivatization, while the tert-butyl carbamate moiety provides orthogonal protection for amine synthesis. Its compatibility with standard coupling reactions and ease of deprotection facilitates efficient access to functionalized cyclobutanes in medicinal chemistry and process development 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 : 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: