3-[Di(methylthio)methylidene]pentane-2,4-dione, with the CAS number 15908-50-6, is an organic compound characterized by its diketone structure, featuring two carbonyl (C=O) groups located at the 2 and 4 positions of a five-carbon chain. The presence of two methylthio groups (-S(CH3)2) at the 3-position contributes to its unique reactivity and properties. This compound is likely to exhibit a range of chemical behaviors typical of diketones, including nucleophilic addition reactions due to the electrophilic nature of the carbonyl carbons. The methylthio substituents can influence the compound's solubility, polarity, and overall stability, potentially making it more reactive than similar diketones without these groups. Additionally, the compound may display interesting spectroscopic characteristics, such as distinct infrared absorption bands corresponding to the carbonyl functionalities and the methylthio groups. Its applications could span various fields, including organic synthesis and materials science, although specific uses may depend on further research into its properties and reactivity.

3-[di(methylthio)methylidene]pentane-2,4-dione

15908-50-6: 3-[Di(methylthio)methylidene]pentane-2,4-dione, with the CAS number 15908-50-6, is an organic compound characterized by its diketone structure, featuring two carbonyl (C=O) groups located at the 2 and 4 positions of a five-carbon chain. The presence of two methylthio groups (-S(CH3)2) at the 3-position contributes to its unique reactivity and properties. This compound is likely to exhibit a range of chemical behaviors typical of diketones, including nucleophilic addition reactions due to the electrophilic nature of the carbonyl carbons. The methylthio substituents can influence the compound's solubility, polarity, and overall stability, potentially making it more reactive than similar diketones without these groups. Additionally, the compound may display interesting spectroscopic characteristics, such as distinct infrared absorption bands corresponding to the carbonyl functionalities and the methylthio groups. Its applications could span various fields, including organic synthesis and materials science, although specific uses may depend on further research into its properties and reactivity.

CAS 15908-50-6

3-[di(methylthio)methylidene]pentane-2,4-dione

2,4-Pentanedione, 3-[bis(methylthio)methylene]-

Ref: IN-DA001QFX

3-[Bis(methylthio)methylene]pentane-2,4-dione

Ref: 54-OR25177

3-(Bis(methylthio)methylene)pentane-2,4-dione

Ref: 10-F723506