2-(Methylsulfanyl)ethyl acetate, with the CAS number 5862-47-5, is an organic compound characterized by its ester functional group. It features a methylthio group (-S-CH3) attached to an ethyl acetate backbone, which contributes to its unique chemical properties. This compound is typically a colorless to pale yellow liquid with a characteristic odor, often associated with fruity or sweet notes due to the acetate moiety. It is moderately soluble in water and more soluble in organic solvents, making it useful in various applications, including as a solvent and in flavoring or fragrance formulations. The presence of the methylthio group can impart distinct sensory characteristics, enhancing its utility in the food and cosmetic industries. Additionally, 2-(methylsulfanyl)ethyl acetate may exhibit low toxicity, but safety precautions should be taken during handling, as with many organic compounds. Its reactivity profile includes potential participation in nucleophilic substitution reactions, making it a versatile intermediate in organic synthesis.

2-(methylsulfanyl)ethyl acetate

5862-47-5: 2-(Methylsulfanyl)ethyl acetate, with the CAS number 5862-47-5, is an organic compound characterized by its ester functional group. It features a methylthio group (-S-CH3) attached to an ethyl acetate backbone, which contributes to its unique chemical properties. This compound is typically a colorless to pale yellow liquid with a characteristic odor, often associated with fruity or sweet notes due to the acetate moiety. It is moderately soluble in water and more soluble in organic solvents, making it useful in various applications, including as a solvent and in flavoring or fragrance formulations. The presence of the methylthio group can impart distinct sensory characteristics, enhancing its utility in the food and cosmetic industries. Additionally, 2-(methylsulfanyl)ethyl acetate may exhibit low toxicity, but safety precautions should be taken during handling, as with many organic compounds. Its reactivity profile includes potential participation in nucleophilic substitution reactions, making it a versatile intermediate in organic synthesis.

CAS 5862-47-5

2-(methylsulfanyl)ethyl acetate

Acetic Acid 2-Methylsulfanyl-Ethyl Ester

Ref: TR-A192720