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(CIS)-4-HYDROXY-2,2,6-TRIMETHYL-CYCLOHEXANONE
SpectraBase Compound ID 5rk9GsOO1pV
InChI InChI=1S/C9H16O2/c1-6-4-7(10)5-9(2,3)8(6)11/h6-7,10H,4-5H2,1-3H3/t6-,7+/m1/s1
InChIKey CSPVUHYZUZZRGF-RQJHMYQMSA-N
Mol Weight 156.22 g/mol
Molecular Formula C9H16O2
Exact Mass 156.11503 g/mol
Enantiomer InChIKey CSPVUHYZUZZRGF-NKWVEPMBSA-N
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 © 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 © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum G4-61-593-3
  • (4R,6S)-4-HYDROXY-2,2,6-TRIMETHYLCYClOHEXANONE
  • (4S,6R)-4-HYDROXY-2,2,6-TRIMETHYL-CYCLOHEXANONE
  • (4S,6R)-2,2,6-trimethyl-4-oxidanyl-cyclohexan-1-one
  • 4-Oxo-cis-3,3,5-trimethyl-cyclohexanol
Title Journal or Book Year
Total Synthesis and Biological Activities of (+)- and (−)-Boscialin and Their 1‘-Epimers Journal of Natural Products 1998
Microbial conversion of 4-oxoisophorone by Aspergillus niger. Agricultural and Biological Chemistry 1988
Microbial conversion of 4-oxoisophorone by thermophile, Thermomonospora curvata. Agricultural and Biological Chemistry 1984

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