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Structure of 52784-32-4
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Methyl 2-oxo-cycloheptanecarboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized cycloheptane scaffolds. The ketone and ester functionalities provide orthogonal handles for selective transformations, including enolate chemistry, nucleophilic additions, and reduction sequences. Its bench-stable nature and compatibility with standard reaction conditions facilitate straightforward incorporation into complex molecular architectures relevant to medicinal chemistry and natural product synthesis.
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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-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: