| Weight | 95.123 g/mol |
|---|---|
| Formula | CH5NO2S |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Methanesulfonamide (3144-09-0)
CH3SO2NH2
Score:
#57 in Medicinal chemistry
,
#7177 in Chemistry
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- Synthesis and biological activity of methanesulfonamide pyrimidine- and N-methanesulfonyl pyrrole-substituted 3,5-dihydroxy-6-heptenoates, a novel series of HMG-CoA reductase inhibitors. (Bioorganic & Medicinal Chemistry, 1997)
- Pilot study of zonisamide (1, 2-benzisoxazole-3-methanesulfonamide) in patients with refractory partial seizures (Epilepsia, 1985)
- Mild Pd-Catalyzed N-Arylation of Methanesulfonamide and Related Nucleophiles: Avoiding Potentially Genotoxic Reagents and Byproducts (Organic Letters, 2011)
- The Novel Neuropeptide Y Y5 Receptor Antagonist Lu AA33810 [N-[[trans-4-[(4,5-Dihydro[1]benzothiepino[5,4-d]thiazol-2-yl)amino]cyclohexyl]methyl]-methanesulfonamide] Exerts Anxiolytic- and Antidepressant-Like Effects in Rat Models of Stress Sensitivity (Journal of Pharmacology and Experimental Therapeutics, 2009)
- DFT based computational study on the molecular conformation, NMR chemical shifts and vibrational transitions for N-(2-methylphenyl) methanesulfonamide and N-(3-methylphenyl) methanesulfonamide (Journal of Molecular Structure, 2010)
- Voltage Dependence of Cardiac Delayed Rectifier Block by Methanesulfonamide Class III Antiarrhythmic Agents (Journal of Cardiovascular Pharmacology, 1994)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - CH3SO2NH2
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SMILESCS(=O)(=O)N
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InChIKeyHNQIVZYLYMDVSB-UHFFFAOYSA-N
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Methanesulfonamide
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