CAS 152142-03-5
:1,2-Ethanediol, 1-(4-chlorophenyl)-, (1R)-
Description:
1,2-Ethanediol, 1-(4-chlorophenyl)-, (1R)-, also known by its CAS number 152142-03-5, is a chemical compound characterized by its structure, which includes a diol functional group and a chlorophenyl substituent. This compound typically exhibits properties associated with both alcohols and aromatic compounds. As a diol, it possesses two hydroxyl (-OH) groups, which contribute to its potential as a solvent and its ability to form hydrogen bonds, enhancing its solubility in polar solvents. The presence of the 4-chlorophenyl group introduces hydrophobic characteristics and can influence the compound's reactivity and interaction with biological systems. The (1R) designation indicates a specific stereochemistry, which can affect the compound's biological activity and physical properties. Generally, compounds of this nature may be utilized in various applications, including pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. Safety and handling considerations are essential, as chlorinated compounds can pose environmental and health risks.
Formula:C8H9ClO2
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Found 4 products.
(1R)-1-(4-chlorophenyl)-1,2-ethanediol
CAS:Formula:C8H9ClO2Color and Shape:SolidMolecular weight:172.6089(1R)-1-(4-Chlorophenyl)-1,2-ethanediol
CAS:<p>(1R)-1-(4-Chlorophenyl)-1,2-ethanediol</p>Purity:95%Molecular weight:172.61g/mol(1R)-1-(4-Chlorophenyl)ethane-1,2-diol
CAS:<p>(1R)-1-(4-Chlorophenyl)ethane-1,2-diol is a chiral molecule that can be found in the racemic form. It is an enantioselective reagent that is used for the hydrolysis of styrene oxide and epoxide. The (1R)-enantiomer has been shown to be more effective than its counterpart in terms of hydrolysis. This compound can be used in bioconversion processes where it is used as a substrate by recombinant bacteria to produce enantiopure (1S,5S)-quinolinium bromide.</p>Formula:C8H9ClO2Purity:Min. 95%Molecular weight:172.61 g/mol
