CAS 134615-24-0

(+)-1-(3-Bromophenyl)ethanol

Description:

(+)-1-(3-Bromophenyl)ethanol is an organic compound characterized by the presence of a bromophenyl group attached to a chiral carbon bearing a hydroxyl (-OH) functional group. This compound features a three-carbon chain with a bromine atom substituted at the para position of the phenyl ring, which influences its chemical reactivity and physical properties. As a chiral molecule, it exists in two enantiomeric forms, with the (+) designation indicating the specific optical activity of this particular isomer. The presence of the hydroxyl group makes it an alcohol, contributing to its solubility in polar solvents and its potential for hydrogen bonding. This compound may exhibit interesting biological activities and can be utilized in various synthetic applications, particularly in the development of pharmaceuticals or agrochemicals. Its unique structural features and chirality make it a subject of interest in both organic chemistry and medicinal chemistry research.

Formula: C₈H₉BrO

InChI: InChI=1S/C8H9BrO/c1-6(10)7-3-2-4-8(9)5-7/h2-6,10H,1H3/t6-/m1/s1

InChI key: InChIKey=ULMJQMDYAOJNCC-ZCFIWIBFSA-N

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

Synonyms:

• (+)-1-(3-Bromophenyl)ethanol
• (1R)-1-(3-Bromophenyl)ethan-1-ol
• (1R)-1-(3-bromophenyl)ethanol
• (R)-3-Bromo-Alpha-Methylbenzyl Alcohol
• (αR)-3-Bromo-α-methylbenzenemethanol
• Benzenemethanol, 3-bromo-α-methyl-, (R)-
• Benzenemethanol, 3-bromo-α-methyl-, (αR)-
• (R)-1-(3-Bromophenyl)ethanol
• (R)-1-(3′-Bromophenyl)ethanol

Benzenemethanol, 3-bromo-a-methyl-, (aR)-

CAS: 134615-24-0

Formula: C₈H₉BrO

Purity: 97%

Color and Shape: Liquid

Molecular weight: 201.0605

Ref: IN-DA00HTCN

(R)-1-(3'-Bromophenyl)ethanol

CAS: 134615-24-0

(R)-1-(3'-Bromophenyl)ethanol

Purity: 97%

Molecular weight: 201.06g/mol

Ref: 54-OR89984

(R)-1-(3-Bromophenyl)ethanol

CAS: 134615-24-0

Formula: C₈H₉BrO

Purity: 97%

Molecular weight: 201.063

Ref: 10-F231612

(R)-1-(3-Bromophenyl)ethanol

CAS: 134615-24-0

(R)-1-(3-Bromophenyl)ethanol is a prochiral ketone that undergoes asymmetric hydrogenation to afford racemic 1-phenylethanol. The catalytic system consists of an ionic liquid, imidazolium salt, and chiral ligands. This catalyst system can be used to transfer hydrogen to the ketone in order to generate two enantiomers with opposite optical rotation.

Formula: C₈H₉BrO

Purity: Min. 95%

Molecular weight: 201.06 g/mol

Ref: 3D-JFA61524