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Structure of 1138480-98-4
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Methyl 6-oxospiro[3.3]heptane-2-carboxylate features a rigid spirocyclic core with a ketone at the bridgehead and an ester group, enabling direct functionalization at C6. This configuration supports efficient access to polycyclic scaffolds through tandem cyclizations and asymmetric transformations under mild conditions.
Methyl 6-oxospiro[3.3]heptane-2-carboxylate serves as a versatile bicyclic building block for the synthesis of complex carbocyclic and heterocyclic frameworks. The spirocyclic core provides rigidity and defined stereochemistry, while the ketone and ester functionalities enable sequential functionalization via enolate chemistry, nucleophilic addition, and reduction. Its bench-stable nature and compatibility with standard synthetic protocols facilitate efficient access to medicinally relevant scaffolds in natural product and medicinal chemistry applications.
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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 : 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: