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Structure of 2320-30-1
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3,5-Dimethylcyclohexanone features a stable cyclohexanone core with two methyl groups positioned at the 3 and 5 ring carbons. This substitution pattern imparts enhanced steric shielding around the carbonyl center, improving resistance to nucleophilic attack. The compound serves as a valuable scaffold in asymmetric synthesis and natural product derivatization due to its defined stereochemical environment and compatibility with standard functional group transformations under mild conditions.
3,5-Dimethylcyclohexanone serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized cyclohexane scaffolds. Its stabilized enolizable α-positions facilitate aldol condensations and nucleophilic additions, while the ketone functionality supports reductive amination, Grignard reactions, and cyclization processes. Bench-stable and amenable to standard purification methods, it functions reliably in multistep syntheses for medicinal chemistry and natural product analogs.
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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#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H225-H319
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P264-P280-P370+P378-P501
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Lot numbers can be found on the outside label of a product: