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N-NITROANILINE
SpectraBase Compound ID 9wPoGeb9CXh
InChI InChI=1S/C6H6N2O2/c9-8(10)7-6-4-2-1-3-5-6/h1-5,7H
InChIKey VBEGHXKAFSLLGE-UHFFFAOYSA-N
Mol Weight 138.13 g/mol
Molecular Formula C6H6N2O2
Exact Mass 138.042927 g/mol
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample E. Kolehmainen, K. Laihia and R. Kauppinen, University of Jyvaskyla, Jyvaskyla, Finland R. Gawinecki and D. Rasala, Pedagogical University, Poland Magn. Reson. Chem. 31, 659(1993)
Solvent Dimethyl sulfoxide-d6; Reference=TMS; Temperature=30C Spectrometer= Jeol GSX 270
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 DMSO-D6
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 DMSO-D6;CR(ACAC)3
  • N-NITRO-PHENYLAMINE;N-NITROANILINE
  • ANILINE, N-NITRO-,
  • N-phenylnitramide
Title Journal or Book Year
Nitramino, NRNO2 (R = H, CH3), as a substituent. 13C and 15N NMR spectroscopic study of nitraminobenzenes and ‐pyridines Magnetic Resonance in Chemistry 1993
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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