CAS 73771-35-4
:3-(methylsulfanyl)benzaldehyde
Description:
3-(Methylsulfanyl)benzaldehyde, with the CAS number 73771-35-4, is an organic compound characterized by the presence of a benzaldehyde functional group and a methylthio substituent at the meta position of the aromatic ring. This compound typically appears as a colorless to pale yellow liquid with a distinct aromatic odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. The presence of the methylthio group imparts unique chemical properties, including potential reactivity in nucleophilic substitution reactions and the ability to participate in various organic synthesis pathways. Additionally, 3-(methylsulfanyl)benzaldehyde may exhibit biological activity, making it of interest in medicinal chemistry and the development of pharmaceuticals. Safety data should be consulted, as with any chemical, to ensure proper handling and usage in laboratory settings. Overall, this compound serves as a valuable intermediate in organic synthesis and research applications.
Formula:C8H8OS
InChI:InChI=1/C8H8OS/c1-10-8-4-2-3-7(5-8)6-9/h2-6H,1H3
SMILES:CSc1cccc(c1)C=O
Synonyms:- Benzaldehyde, 3-(Methylthio)-
- 3-(Methylsulfanyl)benzaldehyde
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Found 4 products.
Benzaldehyde, 3-(methylthio)-
CAS:Formula:C8H8OSPurity:97%Color and Shape:LiquidMolecular weight:152.21353-(Methylthio)benzaldehyde
CAS:<p>3-(Methylthio)benzaldehyde is a molecule that can be used in the preparation of mandelic acid. It has been shown to inhibit the activity of lipase, an enzyme that breaks down fats. The cavity of 3-(methylthio)benzaldehyde has been studied by X-ray analysis and was found to have cationic character with silver ions. It also has functional groups that can be used for protein modification by enzymatic reactions.</p>Formula:C8H8OSPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:152.21 g/mol3-(Methylthio)benzaldehyde
CAS:Formula:C8H8OSPurity:97%Color and Shape:Liquid, OilMolecular weight:152.21



