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Structure of 4255-62-3
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4,4-Dimethylcyclohexanone features a sterically hindered ketone group flanked by two methyl substituents at the 4-position, enhancing its stability and reducing susceptibility to nucleophilic attack. This structural rigidity supports its use in asymmetric synthesis and as a building block for complex cyclic frameworks.
4,4-Dimethylcyclohexanone serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted cyclohexane scaffolds. Its sterically hindered ketone functionality exhibits enhanced stability and facilitates selective reductions, enolizations, and nucleophilic additions. The gem-dimethyl substitution imparts favorable solubility and purification characteristics, making it well-suited for multi-step synthesis and process-scale applications.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1325
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Class : 4.1
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Packing Group : Ⅱ
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Hazard Statements : H228-H319
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Precautionary Statements : P210-P240-P241-P264-P280-P370+P378
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Lot numbers can be found on the outside label of a product: