(S)-1-(3,4-Dimethoxyphenyl)-2-propanol is an organic compound characterized by its chiral structure, which includes a propanol backbone and a substituted phenyl group. The presence of two methoxy groups on the phenyl ring enhances its lipophilicity and can influence its biological activity. This compound typically exists as a colorless to pale yellow liquid or solid, depending on the specific conditions and purity. It is soluble in organic solvents, such as ethanol and dichloromethane, but has limited solubility in water due to its hydrophobic characteristics. The chiral nature of this compound means it can exist in two enantiomeric forms, with the (S)-enantiomer often being of particular interest in pharmacology and medicinal chemistry due to its potential biological activity. The compound may be used in various applications, including as an intermediate in the synthesis of pharmaceuticals or as a research tool in studies of chiral recognition and stereochemistry. Safety data should be consulted for handling and storage, as with any chemical substance.

(S)-1-(3,4-DIMETHOXYPHENYL)-2-PROPANOL

161121-02-4: (S)-1-(3,4-Dimethoxyphenyl)-Propan-2-Ol, (2S)-1-(3,4-dimethoxyphenyl)propan-2-ol

(S)-1-(3,4-Dimethoxyphenyl)-propan-2-ol

1-(3,4-Dimethoxyphenyl)propan-2-ol is a carbonyl compound that is an optical and reaction product. It can be obtained from the reduction of 3,4-dimethoxybenzaldehyde with sodium borohydride in the presence of ethanol. The reduction of 1-(3,4-dimethoxyphenyl)propan-2-ol by kluyveromyces lactis has been shown to have high yield and efficiency. This compound is used as an active substance in pharmaceuticals and as a reagent in organic synthesis. It has also been found to be present at low concentrations in cryptococcus sp. and microorganism isolates.

CAS 161121-02-4: (S)-1-(3,4-DIMETHOXYPHENYL)-2-PROPANOL

(S)-1-(3,4-Dimethoxyphenyl)-propan-2-ol

Ref: 10-F049646

1-(3,4-Dimethoxyphenyl)propan-2-ol

Ref: 3D-FD133284

Benzeneethanol, 3,4-dimethoxy-α-methyl-, (αS)-

Ref: IN-DA001S6T