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Structure of 562-13-0
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This 2,2-dimethylcyclohexane-1,3-dione features a sterically shielded diketone core that enhances stability under standard conditions. The geminal dimethyl groups reduce enolization tendencies and improve handling robustness. This structure integrates readily into cycloaddition reactions and serves as a key intermediate in the synthesis of complex polycyclic scaffolds.
2,2-Dimethylcyclohexane-1,3-dione serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted cyclohexanones and heterocyclic scaffolds. Its diketone functionality supports enolization and subsequent nucleophilic transformations, while the gem-dimethyl substitution enhances stability and modulates reactivity. The compound facilitates one-pot functionalizations and is compatible with standard coupling and cyclization protocols, making it valuable for medicinal chemistry and process development 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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: