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4-METHOXYCARBONYL-ACETANILIDE
SpectraBase Compound ID FxKwGo419hN
InChI InChI=1S/C10H11NO3/c1-7(12)11-9-5-3-8(4-6-9)10(13)14-2/h3-6H,1-2H3,(H,11,12)
InChIKey QKWTXJSLAZKYGV-UHFFFAOYSA-N
Mol Weight 193.2 g/mol
Molecular Formula C10H11NO3
Exact Mass 193.073893 g/mol
Copyright Copyright © 2023-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum H.H.Maurer, M.Meyer, K.Pfleger, A.A. Weber / University of Saarland, D-66424 Homburg Germany
Technique GC/MS
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SRH-2022-3475-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum CJ-0-25-0
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCL3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CH3CN
  • 4-ACETYLAMINO-BENZOIC_ACID-METHYLESTER
  • METHYL-N-ACETYL-4-AMINOBENZOIC-ACID
  • 4-Aminobenzoic acid MEAC @
  • Methyl 4-acetylaminobenzoate
  • 4-Acetamidobenzoic acid methyl ester
  • BENZOIC ACID, 4-(ACETYLAMINO)- METHYL ESTER,
  • Procaine-M (PABA) MEAC
  • Benzocaine-M (PABA) MEAC
  • Dimethocaine-M (PABA) MEAC
Title Journal or Book Year
Nitrogen-15 NMR studies of 5-substituted indoles and 4-substituted acetanilides. Evidence for cross-conjugation effects Magnetic Resonance in Chemistry 1993
Correlation of oxygen-17 substituent-induced chemical shifts:Meta- andpara-substituted methyl benzoates Magnetic Resonance in Chemistry 1992
15N NMR spectroscopy. 30—structure/shift relationships of oligopeptides and copolypeptides, including gramicidin S Organic Magnetic Resonance 1981

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