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3-BETA-CYCLOARTENOL
SpectraBase Compound ID 990SQjDMbNc
InChI InChI=1S/C30H50O/c1-20(2)9-8-10-21(3)22-13-15-28(7)24-12-11-23-26(4,5)25(31)14-16-29(23)19-30(24,29)18-17-27(22,28)6/h9,21-25,31H,8,10-19H2,1-7H3/t21-,22-,23+,24+,25+,27-,28+,29-,30+/m1/s1
InChIKey ONQRKEUAIJMULO-YBXTVTTCSA-N
Mol Weight 426.7 g/mol
Molecular Formula C30H50O
Exact Mass 426.386166 g/mol
Enantiomer InChIKey ONQRKEUAIJMULO-XUPOKUKYSA-N
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum X3-35-618-Cyclo-AE
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6
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 C5D5N
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
  • CYClOARTENOL
  • 9,19-Cyclo-9.beta.-lanost-24-en-3.beta.-ol
Title Journal or Book Year
Chemical constituents of Artocarpus camansi Pharmacognosy Journal 2013
Antibacterial hydroperoxysterols from Xanthosoma robustum Phytochemistry 1996
Separation of 24-Methylenecycloartanol from Cycloartenol Via a Chemical Method Journal of Natural Products 1992
Conformational analysis of cycloartenol, 24-methylenecycloartanol and their derivatives. Agricultural and Biological Chemistry 1989
The Conformation of Cycloartenol Investigated by NMR and Molecular Mechanics Helvetica Chimica Acta 1989

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