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RAC-(5AR,6R,9R,9AS)-4-ACETYL-6-HYDROXY-1-METHOXY-6-METHYL-9-(1-METHYLETHYL)-5A,6,7,8,9,9A-HEXAHYDRODIBENZOFURAN-3-YL-PARA-TOLUENESULFONATE

Compound with spectra: 1 NMR

RAC-(5AR,6R,9R,9AS)-4-ACETYL-6-HYDROXY-1-METHOXY-6-METHYL-9-(1-METHYLETHYL)-5A,6,7,8,9,9A-HEXAHYDRODIBENZOFURAN-3-YL-PARA-TOLUENESULFONATE
SpectraBase Compound ID f1j1WKBbZi
InChI InChI=1S/C26H32O7S/c1-14(2)18-11-12-26(5,28)25-22(18)23-19(31-6)13-20(21(16(4)27)24(23)32-25)33-34(29,30)17-9-7-15(3)8-10-17/h7-10,13-14,18,22,25,28H,11-12H2,1-6H3/t18-,22+,25-,26-/m0/s1
InChIKey IHFOHHAMWLISFS-XQHJKBQKSA-N
Mol Weight 488.6 g/mol
Molecular Formula C26H32O7S
Exact Mass 488.186875 g/mol
Enantiomer InChIKey IHFOHHAMWLISFS-GTKJVGNCSA-N

View Spectrum of RAC-(5AR,6R,9R,9AS)-4-ACETYL-6-HYDROXY-1-METHOXY-6-METHYL-9-(1-METHYLETHYL)-5A,6,7,8,9,9A-HEXAHYDRODIBENZOFURAN-3-YL-PARA-TOLUENESULFONATE

13C NMR Spectrum
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Solvent CDCl3
rac-(5aR,6R,9R,9aS)-4-Acetyl-6-hydroxy-1-methoxy-6-methyl-9-(1-methylethyl)-5a,6,7,8,9,9a-hexahydrodibenzofuran-3-yl p-toluenesulfonate
Title Journal or Book Year
First Total Synthesis of (±)-Linderol A, a Tricyclic Hexahydrodibenzofuran Constituent of Lindera umbellata Bark, with Potent Inhibitory Activity on Melanin Biosynthesis of Cultured B-16 Melanoma Cells The Journal of Organic Chemistry 2003

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