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6,6-DIMETHYL-CIS-2-METHYL-3-OXOBICYCLO-[3.1.1]-HEPTAN,ISOPINOCAMPHON

Compound with spectra: 4 NMR, and 3 MS (GC)

6,6-DIMETHYL-CIS-2-METHYL-3-OXOBICYCLO-[3.1.1]-HEPTAN,ISOPINOCAMPHON
SpectraBase Compound ID 6cH4zCf7gly
InChI InChI=1S/C10H16O/c1-6-8-4-7(5-9(6)11)10(8,2)3/h6-8H,4-5H2,1-3H3/t6-,7+,8-/m1/s1
InChIKey MQPHVIPKLRXGDJ-GJMOJQLCSA-N
Mol Weight 152.24 g/mol
Molecular Formula C10H16O
Exact Mass 152.120115 g/mol
Enantiomer InChIKey MQPHVIPKLRXGDJ-RNJXMRFFSA-N

View Spectrum of 6,6-DIMETHYL-CIS-2-METHYL-3-OXOBICYCLO-[3.1.1]-HEPTAN,ISOPINOCAMPHON

13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCL3

View Spectrum of 6,6-DIMETHYL-CIS-2-METHYL-3-OXOBICYCLO-[3.1.1]-HEPTAN,ISOPINOCAMPHON

13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent Benzene-D6

View Spectrum of 6,6-DIMETHYL-CIS-2-METHYL-3-OXOBICYCLO-[3.1.1]-HEPTAN,ISOPINOCAMPHON

13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.

View Spectrum of 6,6-DIMETHYL-CIS-2-METHYL-3-OXOBICYCLO-[3.1.1]-HEPTAN,ISOPINOCAMPHON

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of 6,6-DIMETHYL-CIS-2-METHYL-3-OXOBICYCLO-[3.1.1]-HEPTAN,ISOPINOCAMPHON

MS (GC) Spectrum
Copyright Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Sample SAFC Cat.no. W227501
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)

View Spectrum of 6,6-DIMETHYL-CIS-2-METHYL-3-OXOBICYCLO-[3.1.1]-HEPTAN,ISOPINOCAMPHON

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum W5-1989-34058-31478

View Spectrum of 6,6-DIMETHYL-CIS-2-METHYL-3-OXOBICYCLO-[3.1.1]-HEPTAN,ISOPINOCAMPHON

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum RCM-8-314-1
  • 2,7,7-Trimethyl-bicyclo(3.1.1)heptan-3-one;isopinocamphone
  • (+)-(1R,2R,5S)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one
  • (+)-Isopinocamphone
  • Pinocamphone<cis->
  • BICYCLO[3.1.1]HEPTAN-3-ONE, 2,6,6-TRIMETHYL-
  • Bicyclo[3.1.1]heptan-3-one, 2,6,6-trimethyl-, (1R,2R,5S)-
6,6-DIMETHYL-TRANS-2-METHYL-3-OXOBICYCLO-[3.1.1]-HEPTAN,PINOCAMPHON
(1S,2R,5R)-2,6,6-Trimethylbicyclo[3.1.1]heptan-3-one
cis-Pinocamphone
(1)-(1alpha,2alpha,5alpha)-2,6,6-trimethylbicyclo(3.1.1)heptan-3-one
Bicyclo[3.1.1]heptane, 3-chloro-2,6,6-trimethyl-
(1R)-NEOISOPINOCAMPHENYLCHLORIDE;(1R)-ENDO-3-CHLORO-2,6,6-TRIMETHYLBICYCLO-[3.1.1]-HEPTANE
ISOPINOCAMPHEYL-BOROHYDRIDE
(-)-Isopinocampheylborane TMEDA complex
(S)-Alpine-Boramine(TM)
Molybdenum, dicarbonyl-bis(.eta.-4-pinocarvone)
TRANS-3-HYDROXY-CIS-2-METHYL-6,6-DIMETHYLBICYCLO-[3.1.1]-HEPTAN,ISOPINOCAMPHEOL
TRANS-3-HYDROXY-TRANS-2-METHYL-6,6-DIMETHYLBICYCLO-[3.1.1]-HEPTAN
CIS-3-HYDROXY-CIS-2-METHYL-6,6-DIMETHYLBICYCLO-[3.1.1]-HEPTAN
Title Journal or Book Year
Carbon-13 nuclear magnetic resonance spectra of pinane monoterpenoids Journal of the Chemical Society, Perkin Transactions 2 1984
cis-Pinocamphone
BICYCLO[3.1.1]HEPTAN-3-ONE, 2,6,6-TRIMETHYL-
6,6-DIMETHYL-TRANS-2-METHYL-3-OXOBICYCLO-[3.1.1]-HEPTAN,PINOCAMPHON
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