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TERT.-BUTYL_2-[(1-S,5-R)-1-HYDROXY-5-ISOPROPENYL-2-METHYL-2-CYCLOHEXENYL]-ACETATE

Compound with spectra: 1 NMR, and 2 MS (GC)

TERT.-BUTYL_2-[(1-S,5-R)-1-HYDROXY-5-ISOPROPENYL-2-METHYL-2-CYCLOHEXENYL]-ACETATE
SpectraBase Compound ID Ge4SJ9LcH1z
InChI InChI=1S/C16H26O3/c1-11(2)13-8-7-12(3)16(18,9-13)10-14(17)19-15(4,5)6/h7,13,18H,1,8-10H2,2-6H3/t13-,16+/m1/s1
InChIKey IVLPSGXYLAWHTN-CJNGLKHVSA-N
Mol Weight 266.38 g/mol
Molecular Formula C16H26O3
Exact Mass 266.188195 g/mol
Enantiomer InChIKey IVLPSGXYLAWHTN-XJKSGUPXSA-N

View Spectrum of TERT.-BUTYL_2-[(1-S,5-R)-1-HYDROXY-5-ISOPROPENYL-2-METHYL-2-CYCLOHEXENYL]-ACETATE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SB-135-720-7

View Spectrum of TERT.-BUTYL_2-[(1-S,5-R)-1-HYDROXY-5-ISOPROPENYL-2-METHYL-2-CYCLOHEXENYL]-ACETATE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum AH-135-720-7

View Spectrum of TERT.-BUTYL_2-[(1-S,5-R)-1-HYDROXY-5-ISOPROPENYL-2-METHYL-2-CYCLOHEXENYL]-ACETATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 2-[(1S,5R)-1-hydroxy-2-methyl-5-(1-methylethenyl)-1-cyclohex-2-enyl]acetic acid tert-butyl ester
6-Allyloxy-6-ethynyl-4-isopropenyl-1-methyl-cyclohexene
(1R,2E,6E,9S,11S)-2,6-Dimethyl-9,11-di(prop-1-en-2-yl)cyclododeca-2,6-dien-1-ylacetate
tert-Butyl (3-oxo-2,3,4,5,6,7-hexahydro-1H-inden-1-yl)acetate
11-(R)-HYDROXY-12-(20)-EN-KNIGHTOL;(1-S,7-R,8-R,11-R,3-E)-18-ACETOXY-7,8-EPOXYCEMBRA-3,12-(20),15-(17)-TRIEN-11-OL
1',2-DIHYDROXY[BICYCLOPENTYL]-2-ACETIC ACID, tert-BUTYL ESTER
ODPCVOSSBGHUTF-SRVKXCTJSA-N
(4aR,8aS)-1,1,6-trimethyl-4a,7,8,8a-tetrahydro-4H-isochromen-3-one
(4aS,8aR)-1,1,6-trimethyl-4a,7,8,8a-tetrahydro-4H-2-benzopyran-3-one
(4aR,8aR)-1,1,6-trimethyl-4a,7,8,8a-tetrahydro-4H-2-benzopyran-3-one
3H-BENZOPYRAN-3-ONE, 1,4,4A,7,8,8A-HEXAHYDRO-1,1,6-TRIMETHYL-
Title Journal or Book Year
Regioselective Isomerisation of Highly Substituted 1-Methylenecyclohexenepoxides to the Corresponding Allylic Alcohols. Influence of the Base and of the Protecting Groups Monatshefte f�r Chemie / Chemical Monthly 2004
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