CAS 14763-61-2
:3-(Methylsulfonyl)phenol
Description:
3-(Methylsulfonyl)phenol, with the CAS number 14763-61-2, is an organic compound characterized by the presence of a phenolic group substituted with a methylsulfonyl group at the meta position. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols due to the presence of the sulfonyl group, which enhances its polarity. The methylsulfonyl group contributes to its potential as a reagent in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. Additionally, 3-(Methylsulfonyl)phenol exhibits antioxidant properties, making it of interest in biochemical research. Its chemical structure allows for various functionalization reactions, which can be exploited in synthetic chemistry. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken. Overall, this compound is notable for its versatility in chemical applications and its relevance in medicinal chemistry.
Formula:C7H8O3S
InChI:InChI=1S/C7H8O3S/c1-11(9,10)7-4-2-3-6(8)5-7/h2-5,8H,1H3
InChI key:InChIKey=MRZXZRGNTXHLKA-UHFFFAOYSA-N
SMILES:S(C)(=O)(=O)C1=CC(O)=CC=C1
Synonyms:- 3-(Hydroxyphenyl) methyl sulfone
- Methyl m-hydroxyphenyl sulfone
- 3-(Methylsulfonyl)phenol
- Phenol, m-(methylsulfonyl)-
- Phenol, 3-(methylsulfonyl)-
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Found 4 products.
PHENOL, 3-(METHYLSULFONYL)-
CAS:Formula:C7H8O3SPurity:97%Color and Shape:SolidMolecular weight:172.20163-Methanesulfonylphenol
CAS:<p>3-Methanesulfonylphenol is a reactive and computationally descriptors, damages, neutralizing, piperidine, vector, oxygen species, molecular descriptors, antioxidant, phenolic lead compound that was synthesized for the purpose of identifying new potential antioxidants. 3-Methanesulfonylphenol has been shown to inhibit the oxidation of lipids and proteins in cells. It also has a strong antioxidant activity against peroxyl radicals and hydroxyl radicals. 3-Methanesulfonylphenol also inhibits the production of hydrogen peroxide by reacting with peroxides in vivo. This results in reduced levels of lipid hydroperoxides and protein carbonyls.</p>Formula:C7H8O3SPurity:Min. 95%Molecular weight:172.2 g/mol



