3-AMINO-2-HYDROXY-N-(4-NITROPHENYL)-PROPANE-1-SULFONAMIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | DWwGnuoiN6a |
|---|---|
| InChI | InChI=1S/C9H13N3O5S/c10-5-9(13)6-18(16,17)11-7-1-3-8(4-2-7)12(14)15/h1-4,9,11,13H,5-6,10H2 |
| InChIKey | LUARXHBURDLTEC-UHFFFAOYSA-N |
| Mol Weight | 275.28 g/mol |
| Molecular Formula | C9H13N3O5S |
| Exact Mass | 275.057592 g/mol |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
3-Azido-N-(4-chlorophenyl)-2-hydroxypropane-1-sulfonamide
4',4''-dibromo-2-oxo-1,3-propanedisulfonanilide
Ethanesulfonamide, N-[4-(2-cyanoacetyl)phenyl]-
N-{4-[(Ethylsulfonyl)amino]phenyl}ethanesulfonamide, N,N'-dimethyl-
CINNAMALDEHYDE-4-(PARA-NITRO-PHENYL)-THIOSEMICARBAZONE
N-[4-[4-[Ethyl(7-fluoroheptyl)amino]butyl]phenyl]methanesulfonamide
1-butyl-1-ethyl-3-(p-nitrophenyl)urea
Sotalol
4'-[1-hydroxy-2-(isopropylamino)ethyl]methanesulfonanilide, hydrochloride
4'-amino-2'-hydroxymethanesulfonanilide
| Title | Journal or Book | Year |
|---|---|---|
| Potential GABAB Receptor Antagonists. VIII. The Synthesis of 3-Amino-N-aryl-2-hydroxy- propane-1-sulfonamides and Analogues of Baclofen Containing Nitro Groups | Australian Journal of Chemistry | 1997 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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