SpectraBase Compound ID | 4mhOpRnzTv6 |
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InChI | InChI=1S/C8H9NO2/c1-6(10)9-7-2-4-8(11)5-3-7/h2-5,11H,1H3,(H,9,10) |
InChIKey | RZVAJINKPMORJF-UHFFFAOYSA-N |
Mol Weight | 151.16 g/mol |
Molecular Formula | C8H9NO2 |
Exact Mass | 151.063329 g/mol |
Copyright | Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved. |
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Source of Spectrum | Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy) |
Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
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Source of Spectrum | CAY-2023-765-0 |
Catalog Number | 22629 |
Title | Journal or Book | Year |
---|---|---|
Metabolites of a Blocked Chloramphenicol Producer | Journal of Natural Products | 2002 |
Advanced Oxidation Chemistry of Paracetamol. UV/H2O2-Induced Hydroxylation/Degradation Pathways and 15N-Aided Inventory of Nitrogenous Breakdown Products. | The Journal of Organic Chemistry | 2002 |
17O NMR studies on substitutedN-arylacetamides and aryl acetates: Torsion angle and electronic effects | Magnetic Resonance in Chemistry | 1988 |
Substituent effects on the N.M.R. spectra of carboxylic acid derivatives. III. Correlation of 13C N.M.R. spectra of para substituted acetanilides and 4'-nitrophenyl 4-substituted benzoates with infrared carbonyl stretching frequencies, 1H N.M.R., rate and equilibrium data | Australian Journal of Chemistry | 1984 |
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