CAS 1572-97-0

(S)-(-)-1-(4-methoxyphenyl)ethanol

Description:

(S)-(-)-1-(4-methoxyphenyl)ethanol, with the CAS number 1572-97-0, is an organic compound characterized by its chiral structure, which includes a methoxy group attached to a phenyl ring and a hydroxyl group on a secondary carbon. This compound is a colorless to pale yellow liquid at room temperature and is known for its aromatic properties due to the presence of the methoxy-substituted phenyl group. It exhibits solubility in organic solvents such as ethanol and ether, while being less soluble in water. The compound's chirality gives rise to distinct optical activity, making it relevant in the field of asymmetric synthesis and pharmaceuticals, where enantiomers can exhibit different biological activities. Additionally, (S)-(-)-1-(4-methoxyphenyl)ethanol can participate in various chemical reactions, including oxidation and esterification, which are important for further functionalization in synthetic organic chemistry. Its applications may extend to fragrance and flavor industries, as well as in the synthesis of more complex organic molecules.

Formula: C₉H₁₂O₂

InChI: InChI=1S/C9H12O2/c1-7(10)8-3-5-9(11-2)6-4-8/h3-7,10H,1-2H3/t7-/m0/s1

InChI key: InChIKey=IUUULXXWNYKJSL-ZETCQYMHSA-N

SMILES: [C@@H](C)(O)C1=CC=C(OC)C=C1

Synonyms:

• (-)-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)-
• (s)-1-(4-methoxyphenyl)ethanol
• (S)-1-(4-Methoxyphenyl)ethanol
• (S)-(-)-4-methoxy-1-(1-hydroxyethyl)benzene

Benzenemethanol, 4-methoxy-α-methyl-, (αS)-

CAS: 1572-97-0

Formula: C₉H₁₂O₂

Purity: 97%

Color and Shape: Liquid

Molecular weight: 152.1904

Ref: IN-DA001PA0

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

CAS: 1572-97-0

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

Purity: 97%

Molecular weight: 152.19g/mol

Ref: 54-OR73206

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

CAS: 1572-97-0

Formula: C₉H₁₂O₂

Purity: 95%

Color and Shape: Liquid, No data available.

Molecular weight: 152.193

Ref: 10-F229496

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

CAS: 1572-97-0

Formula: C₉H₁₂O₂

Purity: >95.0%(GC)

Color and Shape: Colorless to Light yellow clear liquid

Molecular weight: 152.19

Ref: 3B-M3895

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

CAS: 1572-97-0

(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.

Formula: C₉H₁₂O₂

Purity: Min. 95%

Molecular weight: 152.19 g/mol

Ref: 3D-BAA57297