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Structure of 1546875-04-0
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This sulfone-functionalized cyclic carboxylic acid features a rigid, electron-deficient tetrahydrothiophene core that enhances metabolic stability and modulates lipophilicity. The 3-methyl substitution improves crystallinity and solubility in polar solvents, facilitating downstream derivatization. Its bench-stable nature supports direct use in synthetic workflows without protective handling.
3-Methyltetrahydrothiophene-3-carboxylic acid 1,1-dioxide serves as a stable, bench-ready sulfone building block for medicinal chemistry and catalytic synthesis. Its rigid, polarized ring system enables predictable regioselective functionalization and compatibility with standard coupling reactions. The carboxylic acid group facilitates direct derivatization or salt formation, while the sulfonyl moiety enhances metabolic stability and solubility—key attributes in API development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: