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Structure of 585-36-4
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3-(Trifluoromethyl)cyclohexanone features a trifluoromethyl group attached to a cyclohexanone ring, delivering enhanced electron-withdrawing character and metabolic stability. This configuration supports its use in medicinal chemistry scaffolds and as a building block for bioactive molecules requiring high lipophilicity and resistance to oxidative degradation under standard conditions.
3-(Trifluoromethyl)cyclohexanone serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling efficient access to fluorinated cyclic scaffolds. Its trifluoromethyl group imparts enhanced metabolic stability and lipophilicity, while the ketone functionality facilitates nucleophilic additions, reductions, and enolate-based transformations. The compound exhibits good bench stability and is compatible with standard functional group manipulations, making it a practical choice for constructing complex heterocyclic and bioactive molecular frameworks.
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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 : H315-H317-H319-H335
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Precautionary Statements : P261-P264-P271-P272-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: