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Undecacyclo[9.9.0.0(2,9).0(3,7).0(4,20).0(5,18).0(6,16).0(8,15).0(10,14).0(12,19).0(13,17)]icosane-1,6-diol

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

Undecacyclo[9.9.0.0(2,9).0(3,7).0(4,20).0(5,18).0(6,16).0(8,15).0(10,14).0(12,19).0(13,17)]icosane-1,6-diol
SpectraBase Compound ID Jud3EZhY6eP
InChI InChI=1S/C20H20O2/c21-19-13-3-1-2-5(13)9-10-6(2)14-4(1)8-7(3)15(19)11-12(17(9)19)18(10)20(14,22)16(8)11/h1-18,21-22H
InChIKey PBQNETXYBBWYLV-UHFFFAOYSA-N
Mol Weight 292.38 g/mol
Molecular Formula C20H20O2
Exact Mass 292.14633 g/mol

View Spectrum of Undecacyclo[9.9.0.0(2,9).0(3,7).0(4,20).0(5,18).0(6,16).0(8,15).0(10,14).0(12,19).0(13,17)]icosane-1,6-diol

MS (GC) Spectrum
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Source of Spectrum KC-0-1203-21

View Spectrum of Undecacyclo[9.9.0.0(2,9).0(3,7).0(4,20).0(5,18).0(6,16).0(8,15).0(10,14).0(12,19).0(13,17)]icosane-1,6-diol

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum KC-0-1197-21

View Spectrum of Undecacyclo[9.9.0.0(2,9).0(3,7).0(4,20).0(5,18).0(6,16).0(8,15).0(10,14).0(12,19).0(13,17)]icosane-1,6-diol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
1,6-Dibromoundecacyclo[9.9.0.0(2,9).0(3,7).0(4,20).0(5,18).0(6,16).0(8,15).0(10,14).0(12,19).0(13,17)]icosane
Pentacyclo[6.3.0.0(2,6).0(3,10).0(5,9)]undecan-4-ol
Trishomocuban-4-ol
(1beta,5beta,9beta,10beta,11alpha,12beta)-Dodecahydro-10,11-acenaphthylene bis(methanesulfonate)
(1.alpha.,2.alpha.,3.alpha.,3a.beta.,4.beta.,7.beta.,7a.beta.)2,3,3a,4,7,7a-hexahydro-8,8-dimethoxy-4,7-methano-1,2,3-metheno-1H-indene
(1-ALPHA,2-ALPHA,3-ALPHA,3A-ALPHA,4-BETA,7-BETA,7A-BETA)-2,3,3A,4,7,7A-HEXAHYDRO-8,8-DIMETHOXY-4,7-METHANO-1,2,3-METHENO-1H-INDENE
2,4-Methano-4H-inden-4-ol, octahydro-, acetate
2-endo-Hydroxy-2-exo-methyl-4-exo-bromoprotoadamantane
2-Hydroxy-2-noradamantanecarboxylic acid
(8S,20S)-des-A,B-24,24-Difluorocholestane-8.beta.,25-diol
Title Journal or Book Year
Pentagonal dodecahedranes. Novel substitution patterns— MS fragmentation and unsaturation Journal of the Chemical Society, Perkin Transactions 2 1998
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