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CAS 741217-33-4

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(R)-4-Amino-3-(4-fluorophenyl)butanoic acid

Description:
(R)-4-Amino-3-(4-fluorophenyl)butanoic acid, also known as a selective amino acid derivative, is characterized by its chiral center, which contributes to its specific stereochemistry. This compound features an amino group (-NH2), a carboxylic acid group (-COOH), and a fluorophenyl substituent, which enhances its biological activity and solubility properties. The presence of the fluorine atom in the para position of the phenyl ring can influence the compound's lipophilicity and receptor binding affinity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals targeting neurological disorders. The (R) configuration indicates that the amino acid is in its biologically active form, which is crucial for its interaction with biological systems. Additionally, this compound may exhibit properties such as solubility in polar solvents and potential for forming hydrogen bonds, which are important for its reactivity and interaction with other molecules. Overall, (R)-4-Amino-3-(4-fluorophenyl)butanoic acid represents a significant structure in the study of amino acid derivatives and their applications in drug design.
Formula:C10H12FNO2
InChI:InChI=1/C10H12FNO2/c11-9-3-1-7(2-4-9)8(6-12)5-10(13)14/h1-4,8H,5-6,12H2,(H,13,14)/t8-/m0/s1
SMILES:c1cc(ccc1[C@@H](CC(=O)O)CN)F
Synonyms:
  • (3R)-4-Amino-3-(4-fluorophenyl)butanoic acid
  • benzenepropanoic acid, β-(aminomethyl)-4-fluoro-, (betaR)-
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