| Weight | 166.201 g/mol |
|---|---|
| Formula | C8H6O2S |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
Benzo[b]thiophene 1,1-dioxide (825-44-5)
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- Multi-addressable photochromic terarylene containing benzo[b]thiophene-1,1-dioxide unit as ethene bridge: multifunctional molecular logic gates on unimolecular platform (Journal of Materials Chemistry, 2012)
- Synthesis and cytotoxic activity of lipophilic sulphonamide derivatives of the benzo[b]thiophene 1,1-dioxide. (Bioorganic & Medicinal Chemistry, 2004)
- Carbonic anhydrase inhibitors: Inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with benzo[b]thiophene 1,1-dioxide sulfonamides (Bioorganic & Medicinal Chemistry Letters, 2005)
- Structure-based design, synthesis, and biological evaluation of 1,1-dioxoisothiazole and benzo[b]thiophene-1,1-dioxide derivatives as novel inhibitors of hepatitis C virus NS5B polymerase. (Bioorganic & Medicinal Chemistry Letters, 2008)
- 1,3-Dipolar cycloaddition reactions of benzo[b]thiophene 1,1-dioxide with azomethine ylides (Tetrahedron Letters, 2006)
- Novel disperse dyes from benzo[b]thiophene-3(2H)-one-1,1-dioxide and ethyl benzo[b]thien-3(2H)-ylidenecyanoacetate, S, S-dioxide: synthesis and properties (Dyes and Pigments, 2004)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C=CS2(=O)=O
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InChIKeyFRJNKYGTHPUSJR-UHFFFAOYSA-N
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Benzo[b]thiophene 1,1-dioxide
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