Benzenemethanol, 3-methoxy-α-methyl-, (R)-, also known by its CAS number 120523-12-8, is a chiral organic compound characterized by its aromatic structure and functional groups. It features a benzene ring substituted with a methanol group and a methoxy group, along with an α-methyl group, which contributes to its stereochemistry. This compound is typically a colorless to pale yellow liquid with a pleasant odor, and it is soluble in organic solvents while having limited solubility in water. Its chirality indicates that it exists in two enantiomeric forms, with the (R)- configuration being one of them, which can influence its biological activity and interactions. The presence of the methoxy group enhances its lipophilicity, making it relevant in various chemical applications, including pharmaceuticals and agrochemicals. Additionally, its structural features may allow it to participate in various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, making it a versatile compound in organic synthesis.

Benzenemethanol, 3-methoxy-a-methyl-, (R)-

120523-12-8: Benzenemethanol, 3-methoxy-α-methyl-, (R)-, also known by its CAS number 120523-12-8, is a chiral organic compound characterized by its aromatic structure and functional groups. It features a benzene ring substituted with a methanol group and a methoxy group, along with an α-methyl group, which contributes to its stereochemistry. This compound is typically a colorless to pale yellow liquid with a pleasant odor, and it is soluble in organic solvents while having limited solubility in water. Its chirality indicates that it exists in two enantiomeric forms, with the (R)- configuration being one of them, which can influence its biological activity and interactions. The presence of the methoxy group enhances its lipophilicity, making it relevant in various chemical applications, including pharmaceuticals and agrochemicals. Additionally, its structural features may allow it to participate in various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, making it a versatile compound in organic synthesis.

CAS 120523-12-8

Benzenemethanol, 3-methoxy-a-methyl-, (R)-

(1R)-1-(3-METHOXYPHENYL)ETHANOL

Ref: IN-DA008SDJ

(R)-1-(3-methoxyphenyl)ethanol

Ref: 54-OR1064928

(R)-1-(3-Methoxyphenyl)ethan-1-ol

Ref: 3B-M3894