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Structure of 107018-38-2
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1-Cyclohexyl-2,2,2-trifluoroethan-1-ol features a trifluoromethyl group flanked by a hydroxyl-bearing carbon, delivering enhanced lipophilicity and metabolic stability. This bench-stable alcohol integrates readily into synthetic pathways requiring electron-withdrawing substituents, enabling efficient access to fluorinated scaffolds in medicinal chemistry and materials science applications.
1-Cyclohexyl-2,2,2-trifluoroethan-1-ol serves as a stable, bench-friendly building block for fluorinated organic synthesis. Its trifluoromethyl group imparts enhanced metabolic stability and lipophilicity, making it valuable in medicinal chemistry workflows. The primary alcohol functionality enables straightforward derivatization—such as esterification, ether formation, or oxidation—while maintaining compatibility with common protecting group strategies. This compound facilitates the construction of bioactive scaffolds and fluorinated analogs in drug discovery programs.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: