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6,6a-dihydro-1aH-oxireno[a]indene
SpectraBase Compound ID E5KjXpIU2rB
InChI InChI=1S/C9H8O/c1-2-4-7-6(3-1)5-8-9(7)10-8/h1-4,8-9H,5H2
InChIKey UKGCFMYYDATGNN-UHFFFAOYSA-N
Mol Weight 132.16 g/mol
Molecular Formula C9H8O
Exact Mass 132.057515 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.
Source of Spectrum BJO-11-SM3-7
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum GCH-10-910/SM12-arb9
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCL3
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 CDCl3
Copyright Copyright © 2009-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent CCl4
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Research Organic/Inorganic Corporation, Sun Valley, California
Technique CAPILLARY CELL: MELT
  • INDENE OXIDE
  • 1,2-EPOXYINDAN
  • 1AH-OXIRENO/A/INDENE, 6,6A-DIHYDRO-,
  • INDAN, 1,2-EPOXY-,
  • Indan, epoxide
  • 6H-INDENO[1,2-b]OXIRENE, 1A,6A-DIHYDRO-
  • 1,2-Epoxyindane
Title Journal or Book Year
Chiral Fluoro Ketones for Catalytic Asymmetric Epoxidation of Alkenes with Oxone The Journal of Organic Chemistry 2002
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