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1-methyl-6-nitro-1H-indazole
SpectraBase Compound ID GhbY64tkLZH
InChI InChI=1S/C8H7N3O2/c1-10-8-4-7(11(12)13)3-2-6(8)5-9-10/h2-5H,1H3
InChIKey TUWHJYXETJCCPJ-UHFFFAOYSA-N
Mol Weight 177.16 g/mol
Molecular Formula C8H7N3O2
Exact Mass 177.053826 g/mol
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample P. Bouchet, A. Fruchier, G. Joncheray Org. Magn. Resonance 9, 716(1977)
Solvent Dimethyl sulfoxide-d6; Reference=TMS; Temperature=Ambient Spectrometer= Jeol PS-100
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2009-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample A. Fruchier, Institut De Chimie, Fac. Science, Montpellier, France
Solvent CDCl3
Copyright Copyright © 2016-2025 Chemical Block, Russia, Leninsky Prospect 47 - Database Compilation Copyright © 2016-2025 John Wiley & Sons, Inc. All Rights Reserved.
Solvent DMSO-d6
Copyright Copyright © 2022-2025 Chemical Block, Russia, Leninsky Prospect 47 - Database Compilation Copyright © 2022-2025 John Wiley & Sons, Inc. All Rights Reserved.
Solvent DMSO-d6
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample A. Fruchier, Institut De Chimie, Fac. Science, Montpellier, France
Technique KBr WAFER
  • 1H-indazole, 1-methyl-6-nitro-
  • 1-Methyl-6-nitro-indazole
  • 1-METHYL-6-NITROINDAZOL
Title Journal or Book Year
Synthesis of Substituted Pyrazolo[3,4-b]- and Pyrazolo[4,3-c]phenothiazine Derivatives HETEROCYCLES 1995
13C NMR of indazoles Chemistry of Heterocyclic Compounds 1995
N.m.r. studies in the heterocyclic series: XVII—carbon-13 spectra of indazole derivatives Organic Magnetic Resonance 1977

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