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4'-hydroxy-3'-methoxypropiophenone
SpectraBase Compound ID DNTrMBfDpVP
InChI InChI=1S/C10H12O3/c1-3-8(11)7-4-5-9(12)10(6-7)13-2/h4-6,12H,3H2,1-2H3
InChIKey FBGXENQFSMMBNY-UHFFFAOYSA-N
Mol Weight 180.2 g/mol
Molecular Formula C10H12O3
Exact Mass 180.078644 g/mol
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample R. Martin, C. M. Industries, Massy, France
Solvent Chloroform-d; Reference=TMS Spectrometer= Varian CFT-20
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Copyright Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample R. MARTIN, C. M. INDUSTRIES, MASSY, FRANCE
Technique CAPILLARY CELL: MELT (LIQUID PHASE)
Copyright Copyright © 2008-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Methanol
Copyright Copyright © 2008-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Methanol
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum ACI-60-SM13-Figure S12-2
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum LQ-1992-1720-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum LQ-1992-3588-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Va-0-0-0
  • FBGXENQFSMMBNY-UHFFFAOYSA-N
  • 4-HYDROXY-3-METHOXYPROPIOPHENONE
  • 1-(4'-HYDROXY-3'-METHOXYPHENYL)-PROPAN-1-ONE
  • PROPIOPHENONE, 4'-HYDROXY- 3'-METHOXY-,
  • PROPIOPHENONE, 4*-HYDROXY- 3*-METHOXY-,
  • 1-(3-Methoxy-4-oxidanyl-phenyl)propan-1-one
  • 1-(4-hydroxy-3-methoxy-phenyl)propan-1-one
Title Journal or Book Year
Microwave- and ultrasound-assisted semisynthesis of natural methoxylated propiophenones from isomeric mixture of phenylpropenes in minutes Canadian Journal of Chemistry 2005
Anti-AIDS Agents. 48. Anti-HIV Activity of Moronic Acid Derivatives and the New Melliferone-Related Triterpenoid Isolated from Brazilian Propolis Journal of Natural Products 2001

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