CAS 1977-38-4

1-(methylsulfonyl)propan-2-ol

Description:

1-(Methylsulfonyl)propan-2-ol, with the CAS number 1977-38-4, is an organic compound characterized by the presence of a methylsulfonyl group attached to a propan-2-ol backbone. This compound features a hydroxyl (-OH) group, which contributes to its classification as an alcohol, and a sulfonyl group (-SO2-) that enhances its polarity and solubility in water. The molecular structure indicates that it has a chiral center, leading to potential stereoisomerism. Typically, compounds like this exhibit moderate to high boiling points due to hydrogen bonding capabilities associated with the hydroxyl group. Additionally, the presence of the sulfonyl group may impart unique reactivity, making it useful in various chemical syntheses or as a reagent in organic chemistry. Its applications may extend to pharmaceuticals, agrochemicals, or as an intermediate in the synthesis of other chemical compounds. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₄H₁₀O₃S

InChI: InChI=1/C4H10O3S/c1-4(5)3-8(2,6)7/h4-5H,3H2,1-2H3

SMILES: CC(CS(=O)(=O)C)O

1-Methanesulfonylpropan-2-ol

CAS: 1977-38-4

Formula: C₄H₁₀O₃S

Molecular weight: 138.1854

Ref: IN-DA002AZJ

1-Methanesulfonylpropan-2-ol

CAS: 1977-38-4

Methanesulfonylpropan-2-ol is a sulfonic acid that is used in clinical chemistry for the measurement of the concentration of mercaptans. This liquid has an acidic character, which distinguishes it from other sulfonic acids. Methanesulfonylpropan-2-ol also has a magnetic property and can be used to detect the presence of this substance in urine or blood samples.
Methanesulfonylpropan-2-ol is excreted by the kidneys and intestines and is diluted when mixed with water. This substance can be detected using chromatographic science, such as gas chromatography, to identify its presence in biological samples. Methanesulfonylpropan-2-ol may have anticancer properties due to its ability to inhibit cell growth and proliferation. It binds to DNA, disrupting the production of new cells. The intestinal absorption of this drug leads to an increased concentration in the intestine, which may lead to anticancer effects

Formula: C₄H₁₀O₃S

Purity: Min. 95%

Molecular weight: 138.19 g/mol

Ref: 3D-BAA97738