2-(Methylsulfanyl)-1-phenylethanone, also known by its CAS number 5398-93-6, is an organic compound characterized by the presence of a phenyl group and a methylthio group attached to a carbonyl functional group. This compound features a ketone functional group, which is indicative of its reactivity and potential applications in organic synthesis. It typically appears as a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. The methylsulfanyl group contributes to its unique properties, including potential odor characteristics and reactivity in various chemical reactions, such as nucleophilic substitutions or additions. The compound may exhibit moderate solubility in organic solvents, while its solubility in water is generally low due to its hydrophobic nature. Additionally, it may have applications in the synthesis of pharmaceuticals, agrochemicals, or as a flavoring agent, owing to the presence of both the aromatic and sulfur-containing moieties. Safety data should be consulted for handling and storage, as with any chemical substance.

2-(methylsulfanyl)-1-phenylethanone

5398-93-6: 2-(Methylsulfanyl)-1-phenylethanone, also known by its CAS number 5398-93-6, is an organic compound characterized by the presence of a phenyl group and a methylthio group attached to a carbonyl functional group. This compound features a ketone functional group, which is indicative of its reactivity and potential applications in organic synthesis. It typically appears as a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. The methylsulfanyl group contributes to its unique properties, including potential odor characteristics and reactivity in various chemical reactions, such as nucleophilic substitutions or additions. The compound may exhibit moderate solubility in organic solvents, while its solubility in water is generally low due to its hydrophobic nature. Additionally, it may have applications in the synthesis of pharmaceuticals, agrochemicals, or as a flavoring agent, owing to the presence of both the aromatic and sulfur-containing moieties. Safety data should be consulted for handling and storage, as with any chemical substance.

<p>2-(Methylsulfanyl)-1-phenylethan-1-one is a sulfoxide that was synthesized by the photoelectron transfer of methylsulfane. It is an electron acceptor, which can be reduced to the corresponding sulfide or sulfone. It has been shown to react with carbonyl groups and thioacetals, forming triazole derivatives. The molecule has been found to have affinity for aluminium surfaces and has a strong interaction with the carbonyl group.</p>

CAS 5398-93-6

2-(methylsulfanyl)-1-phenylethanone

2-(Methylsulfanyl)-1-phenylethan-1-one

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