| Weight | 191.639 g/mol |
|---|---|
| Formula | C6H6ClNO2S |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
4-Chlorobenzenesulfonamide (98-64-6)
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- Synthesis and in vitro Antitumor Activity of Novel Series 2-Benzylthio-4-chlorobenzenesulfonamide Derivatives. (European Journal of Medicinal Chemistry, 2006)
- CATALYTIC OXIDATION OF ALCOHOLS TO CARBONYL COMPOUNDS MEDIATED BY N-(ARYLSELENO)-4-CHLOROBENZENESULFONAMIDE (Bulletin of the Chemical Society of Japan, 1996)
- Solubility of N-Chloro-4-toluenesulfonamide Sodium and N-Chlorobenzenesulfonamide Sodium in Ethanol, Water, 1-Propanol, and Butan-2-ol (Journal of Chemical & Engineering Data, 2012)
- Comparative Anticonvulsant Activity of 4Chlorobenzenesulfonamide and Prototype Antiepileptic Drugs in Rodents (Epilepsia, 1990)
- Synthesis of N-(2-Benzene-2,2-dichloroethylidene)-4-chlorobenzenesulfonamide and N-(2-Benzene-2,2- dichloroethylidene)-4-methylbenzenesulfonamide (Russian Journal of Organic Chemistry, 2001)
- Measurement and correlation of solubility of N-chlorobenzenesulfonamide sodium and N-chloro-4-toluenesulfonamide sodium in binary ethanol + propan-2-ol mixtures from 278.00 K to 323.00 K (Fluid Phase Equilibria, 2013)
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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(=CC=C1S(=O)(=O)N)Cl
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InChIKeyHHHDJHHNEURCNV-UHFFFAOYSA-N
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4-Chlorobenzenesulfonamide
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