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Home  > 4H-Thieno[2,3-b]thiopyran-2-sulfonamide,5,6-dihydro-4-hydroxy-6-methyl-, 7,7-dioxide

AX16836

120279-26-7 | 4H-Thieno[2,3-b]thiopyran-2-sulfonamide,5,6-dihydro-4-hydroxy-6-methyl-, 7,7-dioxide

Packsize Purity Availability Price Discounted Price    Quantity
5mg 95% in stock $252.00 $176.00 -   +
10mg 95% in stock $449.00 $315.00 -   +
25mg 95% in stock $1,006.00 $705.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AX16836
Chemical Name: 4H-Thieno[2,3-b]thiopyran-2-sulfonamide,5,6-dihydro-4-hydroxy-6-methyl-, 7,7-dioxide
CAS Number: 120279-26-7
Molecular Formula: C8H11NO5S3
Molecular Weight: 297.3716
MDL Number: MFCD09839690
SMILES: OC1CC(C)S(=O)(=O)c2c1cc(s2)S(=O)(=O)N

 

Upstream Synthesis Route
  • The compound $name$ is a versatile building block in chemical synthesis, utilized for its unique structural properties and functional groups. Its 4H-Thieno[2,3-b]thiopyran core provides a conjugated system that can participate in various organic reactions, while the sulfonamide group enhances its reactivity and solubility in polar solvents. In chemical synthesis, $name$ serves as a valuable intermediate for the construction of complex molecules such as pharmaceuticals, agrochemicals, and materials. Its 5,6-dihydro-4-hydroxy-6-methyl- moiety can act as a directing group for selective functionalization reactions, allowing for the precise modification of specific positions on the molecule. Additionally, the 7,7-dioxide functionality offers opportunities for further derivatization, enabling the synthesis of diverse compounds with tailored properties.Overall, $name$ plays a crucial role in the development of novel compounds with potential applications in medicinal chemistry, organic synthesis, and materials science. Its carefully designed structure and functional groups make it a valuable tool for chemists seeking to create custom molecules with specific properties and functions.
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