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de-O-Methylracemosol

Compound with spectra: 3 NMR, and 1 MS (GC)

de-O-Methylracemosol
SpectraBase Compound ID JcmfNClUqrX
InChI InChI=1S/C20H22O4/c1-10-16(22)8-11-4-5-13-12(6-7-15(21)18(13)23)14-9-20(2,3)24-19(10)17(11)14/h6-8,14,21-23H,4-5,9H2,1-3H3
InChIKey VKSWXZSFBSSEFC-UHFFFAOYSA-N
Mol Weight 326.39 g/mol
Molecular Formula C20H22O4
Exact Mass 326.151809 g/mol

View Spectrum of de-O-Methylracemosol

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum AT-47-348-2

View Spectrum of de-O-Methylracemosol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

View Spectrum of de-O-Methylracemosol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6

View Spectrum of de-O-Methylracemosol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • 1,7,8,12B-TETRAHYDRO-2,2,4-TRIMETHYL-2H-BENZO-[6,7]-CYCLOHEPTA-[1,2,3-DE]-[1]-BENZOPYRAN-5,9,10-TRIOL
Racemosol
1,7,8,12B-TETRAHYDRO-2,2,4-TRIMETHYL-2H-BENZO-[6,7]-CYCLOHEPTA-[1,2,3-DE]-[1]-BENZOPYRAN-5,10,11-TRIOL
2-(8-ethoxy-2-oxo-2H-chromen-3-yl)-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-4(3H)-one
5,5'-dichloro-4,4',6,6',7,7'-hexamethoxy-3,3,3',3'-tetramethyl-1,1'-spirobiindan
MORUSIGIN-G
(1,4-Benzenediamine)-tricarbonyl chromium
1-BENZYL-3-[(E)-3-METHOXYCARBONYL-2-PROPENYL]-1H,3H-PYRIDO-[2,1-F]-PURINE-2,4-DIONE
METHYL-13-ISOPROPYL-12-METHOXY-7-OXO-7A-OXA-7-HOMOPODO-CARPA-8,11,13-TRIEN-19-OATE
10-(3-bromophenyl)-6-methoxy-9-methyl-8-oxa-10,12-diazatricyclo[7.3.1.0²,⁷]trideca-2,4,6-trien-11-one
(13R*,13aS*)-7,8,13,13a-Tetrahydro-10,11-dimethoxy-13-phenyl-5H-isoindolo[1,2-b][3]benzazepin-5-one
Title Journal or Book Year
De-O-methylracemosol: A tetracyclic 2,2-dimethylchroman from the roots of Bauhinia racemosa Phytochemistry 1994
Novel Antifungal Tetracyclic Compounds fromBauhinia rufescens LAM. Helvetica Chimica Acta 1991

Wiley Registry of Mass Spectral Data 12th Edition
Author: Wiley

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