CAS 526182-95-6
:2-[4-(Trifluoromethyl)phenyl]piperidine
Description:
2-[4-(Trifluoromethyl)phenyl]piperidine, identified by its CAS number 526182-95-6, is a chemical compound characterized by its piperidine core structure substituted with a trifluoromethylphenyl group. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential applications in medicinal chemistry and material science. The presence of the trifluoromethyl group enhances lipophilicity and can influence the compound's biological activity, making it of interest in drug development. The piperidine ring provides a basic nitrogen atom, which can participate in hydrogen bonding and interact with biological targets. Additionally, the compound's molecular structure suggests potential for various synthetic modifications, allowing for the exploration of structure-activity relationships. Overall, 2-[4-(Trifluoromethyl)phenyl]piperidine is notable for its unique combination of functional groups, which may impart distinctive chemical reactivity and biological properties.
Formula:C12H14F3N
InChI:InChI=1S/C12H14F3N/c13-12(14,15)10-6-4-9(5-7-10)11-3-1-2-8-16-11/h4-7,11,16H,1-3,8H2
InChI key:InChIKey=BPIPNPGHOKSKPH-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=CC=C(C=C1)C2CCCCN2
Synonyms:- 2-[4-(Trifluoromethyl)phenyl]piperidine
- Piperidine, 2-[4-(trifluoromethyl)phenyl]-
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2-[4-(Trifluoromethyl)phenyl]piperidine
CAS:Versatile small molecule scaffoldFormula:C12H14F3NPurity:Min. 95%Molecular weight:229.24 g/mol
