(S)-1-(4-Methoxyphenyl)ethanol

CAS: 1572-97-0

Ref. 3D-BAA57297

Produktinformation

• Name: (S)-1-(4-Methoxyphenyl)ethanol
• Synonyme: (-)-1-(4-Methoxyphenyl)ethanol, (-)-1-(P-Methoxyphenyl)Ethanol, (1S)-1-(4-Methoxyphenyl)Ethanol, (1S)-1-(4-Methoxyphenyl)ethan-1-ol, (Alphas)-4-Methoxy-Alpha-Methylbenzenemethanol, (S)-(-)-1-(P-Methoxyphenyl)Ethanol, (S)-1-(4-Methoxyphenyl)-1-Ethanol, (S)-4-Methoxy-Alpha-Methylbenzyl Alcohol, (S)-4-Methoxy-α-methylbenzyl alcohol, (αS)-4-Methoxy-α-methylbenzenemethanol, Benzenemethanol, 4-methoxy-α-methyl-, (S)-, Benzenemethanol, 4-methoxy-α-methyl-, (αS)-

Beschreibung

(S)-1-(4-Methoxyphenyl)ethanol is an enantiopure chemical compound that is a reaction intermediate in the synthesis of various pharmaceuticals. The reaction system is immobilized, and the biological function of this molecule is activation energy. The surface methodology used for this compound is surface methodology, and the substrate concentration required for the reaction to occur is high. This compound also reacts with water, which may be due to its hydrophilic nature. The strain used in this experiment was Staphylococcus aureus, and the extents of the reaction were determined by measuring the rate at which the substrate concentration decreased over time. (S)-1-(4-Methoxyphenyl)ethanol has an asymmetric synthesis that can be caused by a surfactant or by adding a chiral catalyst to a racemic mixture.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 152.19 g/mol
• Formel: C₉H₁₂O₂
• Reinheit: Min. 95%