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Structure of 130369-09-4
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tert-Butyl ((3-oxocyclobutyl)methyl)carbamate features a cyclobutane ring bearing both a ketone and a carbamate-protected amine, enabling direct incorporation into complex molecular scaffolds. The tert-butyl group ensures stability during synthesis and facilitates straightforward deprotection under mild acidic conditions. This compound serves as a versatile synthon in medicinal chemistry and natural product synthesis.
tert-Butyl ((3-oxocyclobutyl)methyl)carbamate serves as a versatile building block for cyclobutane-containing scaffolds, enabling direct access to functionalized cyclobutyl intermediates. The carbamate group provides excellent stability and ease of removal under mild acidic conditions, while the ketone functionality supports standard transformations including reduction, enolization, and nucleophilic addition. Its compatibility with diverse reaction conditions facilitates integration into complex molecule synthesis, particularly in medicinal chemistry and natural product derivatization 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
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Precautionary Statements : P261-P302+P352
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Lot numbers can be found on the outside label of a product: