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1-O-METHYL-ALPHA-L-RHAMNOPYRANOSIDE
SpectraBase Compound ID AB42PH2HuoG
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-VEIUFWFVSA-N
Mol Weight 178.18 g/mol
Molecular Formula C7H14O5
Exact Mass 178.084124 g/mol
Enantiomer InChIKey OHWCAVRRXKJCRB-PAMBMQIZSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
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 Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
  • METHYL ALPHA-L-RHAMNOPYRANOSIDE
  • METHYL-BETA-L-RHAMNOPYRANOSIDE
Title Journal or Book Year
A Novel Lignan and Flavonoids from Polygonum aviculare Journal of Natural Products 1994
Tricolorin A, Major Phytogrowth Inhibitor from Ipomoea tricolor Journal of Natural Products 1993
New antitumor substances, BE-12406A and BE-12406B, produced by a streptomycete. II. Structure determination. The Journal of Antibiotics 1991
Terpenoid glycosides from Ophiopogon japonicus roots Phytochemistry 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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