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CAS 184844-96-0

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(3R,4R)-1-(Phenylmethyl)-4-(trifluoromethyl)-3-pyrrolidinecarboxylic acid

Description:
(3R,4R)-1-(Phenylmethyl)-4-(trifluoromethyl)-3-pyrrolidinecarboxylic acid is a chiral compound characterized by its pyrrolidine ring structure, which contributes to its stereochemistry and potential biological activity. The presence of a phenylmethyl group enhances its lipophilicity, potentially influencing its interaction with biological membranes and receptors. The trifluoromethyl group is notable for its electronegative properties, which can significantly affect the compound's reactivity and stability, as well as its pharmacokinetic profile. This compound may exhibit unique pharmacological properties, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific receptors or enzymes. Its chiral nature suggests that different enantiomers may have distinct biological activities, which is a critical consideration in drug design. Additionally, the carboxylic acid functional group can participate in hydrogen bonding and ionic interactions, further influencing its solubility and reactivity in various chemical environments. Overall, this compound's structural features suggest potential applications in therapeutic contexts, warranting further investigation into its biological effects and mechanisms of action.
Formula:C13H14F3NO2
InChI:InChI=1S/C13H14F3NO2/c14-13(15,16)11-8-17(7-10(11)12(18)19)6-9-4-2-1-3-5-9/h1-5,10-11H,6-8H2,(H,18,19)/t10-,11-/m0/s1
InChI key:InChIKey=DHLFXWLJSRPJNR-QWRGUYRKSA-N
SMILES:C(N1C[C@H](C(F)(F)F)[C@@H](C(O)=O)C1)C2=CC=CC=C2
Synonyms:
  • (3R,4R)-1-(Phenylmethyl)-4-(trifluoromethyl)-3-pyrrolidinecarboxylic acid
  • 3-Pyrrolidinecarboxylic acid, 1-(phenylmethyl)-4-(trifluoromethyl)-, (3R-trans)-
  • 3-Pyrrolidinecarboxylic acid, 1-(phenylmethyl)-4-(trifluoromethyl)-, (3R,4R)-
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