| Weight | 109.15 g/mol |
|---|---|
| Formula | C2H7NO2S |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Ethanesulfonamide (1520-70-3)
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- SAR Study of a Subtype Selective Allosteric Potentiator of Metabotropic Glutamate 2 Receptor, N-(4-Phenoxyphenyl)-N-(3-pyridinylmethyl)ethanesulfonamide. (Bioorganic & Medicinal Chemistry Letters, 2004)
- Ethenesulfonamide and ethanesulfonamide derivatives, a novel class of orally active endothelin-A receptor antagonists. (Bioorganic & Medicinal Chemistry, 2001)
- Discovery of N-[5-(6-Chloro-3-cyano-1-methyl-1H-indol-2-yl)-pyridin-3-ylmethyl]-ethanesulfonamide, a Cortisol-Sparing CYP11B2 Inhibitor that Lowers Aldosterone in Human Subjects. (Journal of Medicinal Chemistry, 2015)
- N-[3-(1H-Imidazol-4-ylmethyl)phenyl]ethanesulfonamide (ABT-866, 1),1 a Novel 1-Adrenoceptor Ligand with an Enhanced in Vitro and in Vivo Profile Relative to Phenylpropanolamine and Midodrine (Journal of Medicinal Chemistry, 2002)
- The Synthesis and Cyclopolymerization of the N, N-Diallyl- and N, N-Dimethallyl-Derivatives of Methanesulfonamide and Ethanesulfonamide (Journal of Macromolecular Science, Part A, 1972)
- Experimental and theoretical study of the conformational, vibrational and magnetic properties of 4,6-di-O-acetyl-2,3-dideoxy-d-threo-hex-2-enopyranosyl ethanesulfonamide (Journal of Molecular Structure, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCS(=O)(=O)N
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InChIKeyZCRZCMUDOWDGOB-UHFFFAOYSA-N
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