CAS 1517-70-0

(R)-1-(4-Methoxyphenyl)ethanol

Description:

(R)-1-(4-Methoxyphenyl)ethanol, with the CAS number 1517-70-0, 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 typically a colorless to pale yellow liquid at room temperature and exhibits a pleasant aromatic odor due to the presence of the methoxyphenyl group. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water. The presence of the hydroxyl group contributes to its ability to engage in hydrogen bonding, influencing its physical properties and reactivity. As a chiral molecule, it can exist in two enantiomeric forms, with the (R)-configuration being one of them, which may impart specific biological activities or interactions in various chemical reactions. This compound is of interest in the fields of organic synthesis and pharmaceuticals, where its chiral nature can be exploited for the development of enantioselective processes.

Formula: C₉H₁₂O₂

Synonyms:

• (+)-1-(p-Methoxyphenyl)ethanol
• (R)-1-(p-Methoxyphenyl)ethanol
• (alphaR)-4-Methoxy-alpha-methylbenzenemethanol

(R)-1-(4-Methoxyphenyl)ethanol

CAS: 1517-70-0

Formula: C₉H₁₂O₂

Purity: 95%

Color and Shape: Liquid

Molecular weight: 152.1904

Ref: IN-DA003A3Z

(1R)-1-(4-Methoxyphenyl)ethan-1-ol

CAS: 1517-70-0

(1R)-1-(4-Methoxyphenyl)ethan-1-ol

Purity: 97%

Molecular weight: 152.19g/mol

Ref: 54-OR963411

(R)-1-(4-Methoxyphenyl)ethanol

CAS: 1517-70-0

Formula: C₉H₁₂O₂

Purity: 95%

Color and Shape: Liquid

Molecular weight: 152.193

Ref: 10-F229495

(1R)-1-(4-Methoxyphenyl)ethan-1-ol

CAS: 1517-70-0

(1R)-1-(4-Methoxyphenyl)ethan-1-ol (1R,2S)-(+)-N-methylbenzeneethanamine is a stereoselective and selective reagent for the conversion of l-phenylalanine to (2S,3S)-(+)-N-methylbenzeneethanamine. It is commonly used in the synthesis of the enantiopure amino acid l-amino acid derivatives. This compound has been shown to be an effective inhibitor of bacterial growth at high concentrations. The reaction rate increases with increasing temperature and substrate concentration. The cell membrane permeability is higher than that of styrene, which makes this compound useful for the preparation of immobilized enzymes for carbonyl reduction reactions.

Formula: C₉H₁₂O₂

Purity: Min. 95%

Molecular weight: 152.19 g/mol

Ref: 3D-BAA51770