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METHYL-ALPHA-L-RHAMNOSID
SpectraBase Compound ID KA97WGULvOE
InChI InChI=1S/C7H14O5/c1-3-4(8)5(9)6(10)7(11-2)12-3/h3-10H,1-2H3/t3-,4-,5+,6+,7-/m1/s1
InChIKey OHWCAVRRXKJCRB-ULQPCXBYSA-N
Mol Weight 178.18 g/mol
Molecular Formula C7H14O5
Exact Mass 178.084124 g/mol
Enantiomer InChIKey OHWCAVRRXKJCRB-TYDWOXHJSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
  • ALPHA-L-RHA-OME
  • METHYL ALPHA-L-RHAMNOPYRANOSIDE
Title Journal or Book Year
1H and13C NMR Data for 3-O-, 4-O- and 3,4-Di- 1O-glycosylated Methyl α-L-Rhamnopyranosides Magnetic Resonance in Chemistry 1997
Structure Elucidation of Three Triterpenoid Saponins from Alphitonia zizyphoides Using 2D Nmr Techniques Journal of Natural Products 1994
NMR and conformational study of branched oligosaccharides containing 2,3-disubstituted residues of α-L-rhamnose Canadian Journal of Chemistry 1990
Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon-13 nuclear magnetic resonance spectroscopy Journal of the American Chemical Society 1978

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