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CAS 213995-12-1

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(R)-2-Piperidinyl-1,1,2-triphenylethanol

Description:
(R)-2-Piperidinyl-1,1,2-triphenylethanol is a chiral compound characterized by its piperidine ring and a triphenylethanol moiety. This substance features a piperidine nitrogen atom that contributes to its basicity and potential for forming hydrogen bonds, which can influence its solubility and reactivity. The presence of three phenyl groups attached to the ethanol backbone enhances its hydrophobic character, making it less soluble in polar solvents while potentially increasing its affinity for lipid membranes. The chirality of the compound, indicated by the (R) configuration, suggests that it may exhibit specific biological activity or selectivity in interactions with biological targets, such as receptors or enzymes. This compound may be of interest in medicinal chemistry for its potential applications in drug development, particularly in the design of pharmaceuticals that require specific stereochemistry for optimal efficacy. Additionally, its structural features may allow for various synthetic modifications, making it a versatile building block in organic synthesis.
Formula:C25H27NO
InChI:InChI=1/C25H27NO/c27-25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24(21-13-5-1-6-14-21)26-19-11-4-12-20-26/h1-3,5-10,13-18,24,27H,4,11-12,19-20H2/t24-/m1/s1
SMILES:c1ccc(cc1)[C@H](C(c1ccccc1)(c1ccccc1)O)N1CCCCC1
Synonyms:
  • (R)-()-2-Piperdinyl-1,1,2-triphenylethanol
  • (2S)-1,1,2-triphenyl-2-piperidin-1-ylethanol
  • 1-[(1R)-2-hydroxy-1,2,2-triphenylethyl]piperidinium
  • (2R)-1,1,2-triphenyl-2-piperidin-1-ylethanol
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