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Structure of 58113-36-3
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This piperidine derivative features a bis(4-fluorophenyl)methylene bridge, conferring enhanced lipophilicity and metabolic stability. The electron-deficient aromatic system enables robust π–π interactions in target binding, while the tertiary nitrogen integrates readily into diverse molecular architectures. Bench-stable under standard conditions, it serves as a key scaffold for medicinal chemistry campaigns targeting CNS receptors and kinase modulators.
4-(Bis(4-fluorophenyl)methylene)piperidine serves as a versatile building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its conjugated enamine system enables efficient Michael additions and electrophilic functionalization, while the piperidine core offers a handle for further derivatization. The molecule exhibits good bench stability and facilitates purification via standard chromatographic methods, making it suitable for scalable synthetic workflows in medicinal chemistry and process development.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: