| Weight | 186.236 g/mol |
|---|---|
| Formula | C7H10N2O2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
4-Amino-3-methylbenzenesulfonamide (53297-70-4)
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- Synthesis and anti-HIV activity of N-(3-amino-3,4-dihydro-4-oxopyrimidin-2-yl)-4-chloro-2-mercapto-5-methylbenzenesulfonamide derivatives (Journal of Heterocyclic Chemistry, 2007)
- The method of N- [4- [5- (cyclopentyloxycarbonyl) amino-1-methyl-indol-3-yl-methyl] -3-methoxybenzoyl] for preparing a pharmaceutical composition containing the physical form of the composition -2-methylbenzenesulfonamide (1991)
- Method N 4- 5- (cyclopentyloxycarbonyl) amino-1-methyl-indol-3-yl-methyl | -3-methoxybenzoyl | -2-methylbenzenesulfonamide phys ikaalista valmistamiseks containing pharmaceutical form of the composition i (1991)
- N- / 4- / 5- (cyclopentyloxycarbonyl) amino-1-methyl-indol-3-ylmethyl / -3-methoxybenzoyl / pharmaceutical composition containing the physical form -2-methylbenzenesulfonamide (1998)
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SMILESCC1=C(C=CC(=C1)S(=O)(=O)N)N
-
InChIKeyIGQGXIVCGKMRAM-UHFFFAOYSA-N
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