CAS 23508-35-2
:(S)-3-(4-Hydroxyphenyl)-2-hydroxypropionic acid
Description:
(S)-3-(4-Hydroxyphenyl)-2-hydroxypropionic acid, also known as L-DOPA, is an important organic compound with significant biological relevance. It is a chiral molecule, meaning it exists in two enantiomeric forms, with the (S) configuration being the biologically active form. This compound features a phenolic hydroxyl group, which contributes to its reactivity and solubility in polar solvents. L-DOPA is primarily recognized for its role as a precursor to neurotransmitters such as dopamine, norepinephrine, and epinephrine, making it crucial in the treatment of Parkinson's disease and other neurological disorders. The presence of both hydroxyl groups enhances its ability to form hydrogen bonds, influencing its interactions in biological systems. Additionally, L-DOPA exhibits antioxidant properties, which may provide protective effects against oxidative stress in neuronal tissues. Its pharmacological applications, coupled with its structural characteristics, make it a compound of interest in both medicinal chemistry and neurobiology.
Formula:C9H10O4
InChI:InChI=1/C9H10O4/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1-4,8,10-11H,5H2,(H,12,13)/t8-/m0/s1
SMILES:c1cc(ccc1C[C@@H](C(=O)O)O)O
Synonyms:- (2S)-2-Hydroxy-3-(4-hydroxyphenyl)propanoic acid
- (S)-3-(4-Hysroxyphenyl)-2-hydroxypropionoicacid
- Benzenepropanoic acid, alpha,4-dihydroxy-, (alphaS)-
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Found 5 products.
Benzenepropanoic acid, α,4-dihydroxy-, (αS)-
CAS:Formula:C9H10O4Purity:98%Color and Shape:SolidMolecular weight:182.1733(S)-3-(4-Hydroxyphenyl)lactic acid
CAS:(S)-3-(4-Hydroxyphenyl)lactic acidPurity:≥98%Molecular weight:182.17g/mol(S)-3-(4-Hydroxyphenyl)lactic acid
CAS:<p>(S)-3-(4-Hydroxyphenyl)lactic acid is a Leuconostoc mesenteroides metabolite with antioxidant properties.</p>Formula:C9H10O4Purity:99.78%Color and Shape:SolidMolecular weight:182.17(S)-3-(4-Hydroxyphenyl)-2-hydroxypropionic acid
CAS:<p>(S)-3-(4-Hydroxyphenyl)-2-hydroxypropionic acid is a phenolic compound that is used in the synthesis of streptavidin. It is prepared by reacting p-hydroxybenzoic acid with tyrosol. The ester linkage between the two molecules is formed by an amide reaction with sodium carbonate, followed by solvent removal and purification. The solvents are removed using sodium carbonate, which allows for the formation of an o-benzyl-l-tyrosine ester linkage. This product has a constant boiling point of 177 degrees Celsius at atmospheric pressure and can be used in organic chemistry as a solvent or reagent.</p>Formula:C9H10O4Purity:Min. 95%Color and Shape:PowderMolecular weight:182.17 g/mol(S)-3-(4-Hydroxyphenyl)-2-hydroxypropionic acid
CAS:Formula:C9H10O4Purity:98%Color and Shape:SolidMolecular weight:182.175




