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Structure of 16205-98-4
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3-Oxocyclohexanecarboxylic acid features a conjugated keto-carboxylic acid motif within a cyclohexane ring, enabling direct participation in Michael additions and decarboxylation cascades. The α,β-unsaturated system facilitates efficient coupling with nucleophiles under mild conditions, while the cyclic scaffold imparts rigidity that enhances regioselectivity in synthetic transformations. This compound serves as a key intermediate for bioactive heterocycles and natural product analogs.
3-Oxocyclohexanecarboxylic acid serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized cyclohexane scaffolds. Its α,β-unsaturated carbonyl system facilitates Michael additions, aldol reactions, and cyclizations under mild conditions. The molecule exhibits bench stability, ease of purification, and compatibility with common protecting groups, making it valuable for medicinal chemistry and natural product synthesis 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-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: