CAS 131864-71-6
:(S)-1-(2-chlorophenyl)ethanol
Description:
(S)-1-(2-chlorophenyl)ethanol, with the CAS number 131864-71-6, is an organic compound characterized by its chiral structure, which includes a hydroxyl group (-OH) attached to a carbon atom that is also bonded to a 2-chlorophenyl group. This compound typically exhibits properties associated with alcohols, such as being a polar molecule due to the presence of the hydroxyl group, which can engage in hydrogen bonding. The 2-chlorophenyl substituent introduces a degree of hydrophobicity and can influence the compound's reactivity and solubility in various solvents. The chirality of the molecule means it exists in two enantiomeric forms, with the (S)-configuration being one of them, which can have implications for its biological activity and interactions. This compound may be of interest in pharmaceutical applications, particularly in the development of chiral drugs, as well as in organic synthesis where specific stereochemistry is required. Its physical properties, such as boiling point and melting point, would depend on the molecular interactions and the presence of functional groups.
Formula:C8H9ClO
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Found 5 products.
(S)-1-(2-Chlorophenyl)ethanol, 98%
CAS:<p>It is an intermediate in organic syntheses and used as a pharmaceutical intermediates. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / ite</p>Formula:C8H9ClOPurity:98%Molecular weight:156.61Benzenemethanol, 2-chloro-α-methyl-, (αS)-
CAS:Formula:C8H9ClOPurity:98%Color and Shape:LiquidMolecular weight:156.6095(S)-1-(2-Chlorophenyl)ethanol
CAS:(S)-1-(2-Chlorophenyl)ethanolPurity:98%Molecular weight:156.61g/mol(S)-1-(2-Chlorophenyl)ethanol
CAS:<p>(S)-1-(2-Chlorophenyl)ethanol is a substrate for the enzyme dehydrogenase, which catalyzes the conversion of (R)-1-(2-chlorophenyl)ethanol to (R)-1-(2-chlorophenyl)propanol. The reaction time for this reaction is dependent on the concentration of the substrate, with high concentrations of (S)-1-(2-chlorophenyl)ethanol requiring a longer reaction time. The product, (R)-1-(2-chlorophenyl)propanol, is an organic chemical that can be used as a model system for studying other reactions involving alcohols. This compound has been shown to be reactive in biological systems and has been found to have symptoms similar to those of Parkinson's disease in mice.</p>Formula:C8H9ClOPurity:Min. 95%Molecular weight:156.61 g/mol




