(S)-(+)-a-Methoxyphenylacetic acid

CAS: 26164-26-1

Ref. 3D-FM25336

Produktinformation

• Name: (S)-(+)-a-Methoxyphenylacetic acid
• Synonyme: L-a-Methoxyphenylacetic acid(S)-2-Methoxy-2-(phenyl)ethanoic acid(S)-(+)-O-Methylmandelic acid, (+)-2-Methoxy-2-phenylacetic acid, (+)-2-Methoxyphenylacetic acid, (+)-Methoxyphenylacetic acid, (+)-α-Methoxyphenylacetic acid, (2S)-Methoxy(phenyl)acetate, (2S)-Methoxy(phenyl)ethanoic acid, (2S)-O-Methylmandelic acid, (2S)-methoxy(phenyl)ethanoate, (S)-(+)-2-Methoxy-2-phenylacetic acid, (S)-(+)-Alpha-Methoxyphenylacetic Acid, (S)-(+)-Methoxyphenylacetic acid, (S)-(+)-O-Methylmandelic acid, (S)-2-Methoxy-2-(phenyl)ethanoic acid, (S)-2-Methoxyphenylacetic acid, (S)-α-Methoxy-α-phenylacetic acid, (S)-α-Methoxybenzeneacetic acid, (S)-α-Methoxybenzeneethanoic acid, (αS)-α-Methoxybenzeneacetic acid, <span class="text-smallcaps">L</span>-α-Methoxyphenylacetic acid, Acetic acid, methoxyphenyl-, (S)-, Benzeneacetic acid, α-methoxy-, (S)-, Benzeneacetic acid, α-methoxy-, (αS)-, benzeneacetic acid, alpha-methoxy-, ion(1-), (alphaS)-

Beschreibung

(S)-(+)-a-Methoxyphenylacetic acid is a chiral primary amine. It is used in the preparation of monomers, and as a reagent for the synthesis of other compounds. The enantiomer of (S)-(+)-a-methoxyphenylacetic acid has been synthesized and characterized by NMR spectroscopy and conformational analysis. The molecule exists as a mixture of two conformers, one with the phenyl group on the left side and the other with it on the right side. The conformation that is observed depends on which enantiomer is used; there are no restrictions to rotation about any single bond in either conformer.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 166.17 g/mol
• Formel: C₉H₁₀O₃
• Reinheit: Min. 95%