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Structure of 902836-91-3
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This piperidine derivative features a trifluoromethyl-substituted phenoxy moiety, delivering enhanced lipophilicity and metabolic stability. The electron-withdrawing trifluoromethyl group modulates electronic properties, improving binding affinity in target-directed pharmacophores. Designed for medicinal chemistry applications, it integrates readily into bioactive scaffolds requiring controlled distribution and prolonged residence time.
3-(4-(Trifluoromethyl)phenoxy)piperidine serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through standard functionalization protocols. Its trifluoromethylphenyl ether moiety enhances metabolic stability and lipophilicity, while the piperidine core offers a readily derivatizable nitrogen for salt formation or conjugation. Bench-stable and compatible with common coupling reactions, it facilitates efficient synthesis of CNS-targeted compounds and receptor modulators.
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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-H319
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: