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Structure of 695-95-4
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Methyl 3-oxocyclobutanecarboxylate features a strained cyclobutane ring with a conjugated ketone and ester group, enabling facile functionalization at the 3-position. This reactive scaffold integrates readily into synthetic sequences requiring controlled ring opening or nucleophilic addition, particularly in the construction of bioactive heterocycles and natural product analogs under mild conditions.
Methyl 3-oxocyclobutanecarboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized cyclobutane scaffolds. Its α,β-unsaturated ketone motif facilitates Michael additions, aldol reactions, and metal-catalyzed cyclizations. The ester group provides a handle for selective transformations, while the cyclic ketone exhibits robust bench stability and compatibility with diverse reaction conditions. This compound functions effectively in the synthesis of bioactive heterocycles and natural product analogs.
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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-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: