2,2,4,4-Tetramethylthietan-3-one is a cyclic sulfur-containing compound characterized by its unique thietan ring structure, which includes a ketone functional group. This compound features a four-membered ring with two methyl groups attached to both the second and fourth carbon atoms, contributing to its steric bulk and potentially influencing its reactivity and physical properties. It is typically a colorless to pale yellow liquid with a distinctive odor. The presence of the ketone group suggests that it may participate in various chemical reactions, such as nucleophilic additions or reductions. Its molecular structure may impart specific characteristics such as solubility in organic solvents and moderate stability under standard conditions. Additionally, due to the presence of sulfur, it may exhibit unique properties compared to non-sulfur analogs, including potential reactivity with electrophiles. As with many organic compounds, safety data should be consulted to understand its handling and potential hazards. Overall, 2,2,4,4-tetramethylthietan-3-one is of interest in organic synthesis and may have applications in various chemical processes.

2,2,4,4-tetramethylthietan-3-one

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2,2,4,4-TETRAMETHYLTHIETAN-3-ONE

2,2,4,4-Tetramethylthietan-3-one

2,2,4,4-Tetramethylthietan-3-one is a triene and an ether. It is prepared by the reaction of acetone with trimethylsilyl chloride in the presence of benzene in a sulphenic solvent. 2,2,4,4-Tetramethylthietan-3-one can be used to prepare penicillin anhydride by refluxing it with penicillin and an acid anhydride in the presence of a base. 2,2,4,4-Tetramethylthietan-3-one is also used in the synthesis of norbornene.

CAS 58721-01-0: 2,2,4,4-tetramethylthietan-3-one

2,2,4,4-TETRAMETHYLTHIETAN-3-ONE

Ref: 10-F540042

2,2,4,4-Tetramethylthietan-3-one

Ref: 54-OR961512

2,2,4,4-Tetramethylthietan-3-one

Ref: 3D-ICA72101