SpectraBase Compound ID | 1DacV2v3LFv |
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InChI | InChI=1S/C8H8O2/c1-7(9)10-8-5-3-2-4-6-8/h2-6H,1H3 |
InChIKey | IPBVNPXQWQGGJP-UHFFFAOYSA-N |
Mol Weight | 136.15 g/mol |
Molecular Formula | C8H8O2 |
Exact Mass | 136.052429 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 Sample | SAFC Cat.no. 108723 |
Source of Spectrum | Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy) |
Title | Journal or Book | Year |
---|---|---|
Electron-Withdrawing Substituents Decrease the Electrophilicity of the Carbonyl Carbon. An Investigation with the Aid of 13C NMR Chemical Shifts, ν(CO) Frequency Values, Charge Densities, and Isodesmic Reactions To Interprete Substituent Effects on Reactivity | The Journal of Organic Chemistry | 2002 |
Determination of aromaticity indices of thiophene and furan by nuclear magnetic resonance spectroscopic analysis of their phenyl esters | Journal of Heterocyclic Chemistry | 2002 |
17O NMR studies on substitutedN-arylacetamides and aryl acetates: Torsion angle and electronic effects | Magnetic Resonance in Chemistry | 1988 |
Oxygen-17 NMR chemical shifts of esters | Organic Magnetic Resonance | 1984 |
Substituent effect treatment of interactions between contiguous functionalities G-X. 2. Remote response to polar-inductive and mesomeric influence of X on G = -O- and -NH- | The Journal of Organic Chemistry | 1980 |
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