2-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)ethyl methanesulfonate
$350.00
CAS No.: 1010836-46-0
Catalog No.: 195463
Purity: 95%
MF: C7H14O5S2
MW: 242.318
Storage: 2-8 degree Celsius
SMILES: CS(=O)(=O)OCC1CCS(CC1)(=O)=O
Catalog No.: 195463
Purity: 95%
MF: C7H14O5S2
MW: 242.318
Storage: 2-8 degree Celsius
SMILES: CS(=O)(=O)OCC1CCS(CC1)(=O)=O
2-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)ethyl methanesulfonate; CAS No.: 1010836-46-0; 2-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)ethyl methanesulfonate. PROPERTIES: 2-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)ethyl methanesulfonate appears as a colorless to pale yellow liquid with a slight odor. Its molecular formula is C8H14O5S2, corresponding to a molecular weight of approximately 262.33 g/mol. The compound exhibits a boiling point around 150-155 C at 760 mmHg and a density of about 1.25 g/cm? at 25 C. It demonstrates moderate solubility in common organic solvents such as methanol, acetone, and diethyl ether but is sparingly soluble in water. The substance is sensitive to strong bases and Lewis acids, which may cause sulfonate hydrolysis or ring-opening reactions. Proper storage requires keeping it in a tightly sealed, amber glass container in a cool, dry location away from direct sunlight and heat sources. The temperature should be maintained below 10 C if possible. Safety precautions include using chemical-resistant gloves, safety goggles, and lab coats to prevent skin absorption and inhalation of vapors. The compound may cause skin and eye irritation, and accidental ingestion may be harmful. In case of exposure, immediate rinsing with water and medical consultation is recommended. APPLICATIONS: 2-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)ethyl methanesulfonate serves as a valuable intermediate in the synthesis of pharmaceuticals, particularly in the preparation of certain antibacterial and antifungal agents. Its sulfonate and thiopyran groups provide structural features important for receptor binding and bioactivity. In biochemical research, it functions as a building block for creating enzyme inhibitors and prodrugs. Additionally, it finds application in the development of fluorescent probes for bioimaging, where its sulfonate group allows for selective labeling of biological targets such as proteins and lipids. The compound is also employed in the synthesis of agrochemicals, though specific applications in this area are limited to non-agricultural research settings.
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