3-Azido-2-hydroxy-N-(4-nitrophenyl)propane-1-sulfonamide
Compound with spectra: 1 NMR, and 1 MS (GC)
| SpectraBase Compound ID | 3Fei2aJcFUW |
|---|---|
| InChI | InChI=1S/C9H11N5O5S/c10-13-11-5-9(15)6-20(18,19)12-7-1-3-8(4-2-7)14(16)17/h1-4,9,12,15H,5-6H2 |
| InChIKey | VWJHCLPXWRGEKB-UHFFFAOYSA-N |
| Mol Weight | 301.28 g/mol |
| Molecular Formula | C9H11N5O5S |
| Exact Mass | 301.04809 g/mol |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | B-50-23-21 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
3-azido-2-hydroxy-N-(4-methoxyphenyl)propane-1-sulfonamide
N-(4-CHLOROPHENYL)-3-(1,1-DIMETHYLETHYLAMINO)-2-HYDROXY-PROPANE-1-SULFONAMIDE
N-(4-chlorophenyl)-3-(1,1-dimethylethylamino)-2-hydroxypropane-1-sulfonamide hydrochloride
N-(4-NITROPHENYL)-BENZENESULFONAMIDE
N-cyclohexyl-N'-(p-nitrophenyl)sulfamide
N,N-Bis(methylsulfonyl)-4-nitro-aniline
N-(4-butylphenyl)(phenyl)methanesulfonamide
Propanoic acid, 3-hydroxy-2-(hydroxymethyl)-2-methyl-, 2-[4-[(methylsulfonyl)amino]phenyl]hydrazide
N-(4-Aminophenyl)-4-methylbenzenesulfonamide
N-(3-chloro-4-methylphenyl)ethanesulfonamide
| 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 |
Wiley Registry of Mass Spectral Data 12th Edition
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Wiley Registry of Mass Spectral Data 2023
Author: Wiley
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