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Structure of 198995-91-4
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Benzyl 3-oxocyclobutanecarboxylate features a strained cyclobutane ring bearing a ketone and ester functionality, enabling direct functionalization at the 3-position. This scaffold integrates readily into complex molecular architectures under mild conditions, offering high reactivity for C–C bond formation and serving as a key building block in synthetic organic chemistry workflows.
Benzyl 3-oxocyclobutanecarboxylate serves as a versatile synthon in organic synthesis, enabling efficient access to functionalized cyclobutane scaffolds. The ketone and ester functionalities exhibit robust compatibility with standard transformations, including enolate chemistry and nucleophilic additions. Its bench-stable nature and straightforward purification support reliable use in multistep sequences, particularly for constructing bioactive heterocycles and cyclic intermediates in medicinal chemistry workflows.
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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 : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: