N-(BENZOYL)-ALPHA-(PHENYLSULFONYL)-2-FLUOROBENZYLAMINE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | FugxsmMy4hT |
|---|---|
| InChI | InChI=1S/C20H16FNO3S/c21-18-14-8-7-13-17(18)20(22-19(23)15-9-3-1-4-10-15)26(24,25)16-11-5-2-6-12-16/h1-14,20H,(H,22,23) |
| InChIKey | CTEWPGFEYAZHNT-UHFFFAOYSA-N |
| Mol Weight | 369.41 g/mol |
| Molecular Formula | C20H16FNO3S |
| Exact Mass | 369.083493 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1-(3,4-dimethoxyphenyl)-2-methylpropan-2-yl phenyl(phenylsulfonyl)methylcarbamate
2-(1-tosylethyl)benzenesulfonic acid fluoromethyl ester
(+)-2-(m-Tolyl)-2,3-dihydrobenzo[b]thiophene 1,1-dioxide
2-(2-(Naphthalen-2-yl)-2-(phenylsulfonyl)ethyl)oxirane
2,3-Diphenyl-2,4-dihydro-1,3-benzothiazine
2,3,4,5-Tetrafluoro-6-(benzylcarbamoyl)benzoic acid
(E)-1-[2-(Benzylsulfonyl)phenyl]-1-nitro-2-(3-thienyl)ethene
2-[1-(Toluene-4-sulfonyl)-vinyl]-benzenesulfonic acid, ethyl ester
1-(4-fluorophenyl)-3-(5-methyl-2-furyl)-3-(phenylsulfonyl)-1-propanone
(+)-Pinacol (+-)-1-benzamido-1-(2-methoxyphenyl)methaneboronate
| Title | Journal or Book | Year |
|---|---|---|
| Inorganic base-catalyzed formation of antivirally active N-substituted benzamides from α-amido sulfones and N-nucleophile | Chemistry Central Journal | 2011 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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