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HOVAGTYPODGVJG-XUUWZHRGSA-N
SpectraBase Compound ID 3KSelv1z9Lk
InChI InChI=1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6-,7-/m1/s1
InChIKey HOVAGTYPODGVJG-XUUWZHRGSA-N
Mol Weight 194.18 g/mol
Molecular Formula C7H14O6
Exact Mass 194.079038 g/mol
Enantiomer InChIKey HOVAGTYPODGVJG-ZYNSJIGGSA-N
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample K. Bock, C. Pedersen J. Chem. Soc. Perkin Trans. Ii, 1974, 293
Solvent Deuterium oxide; Reference=Dioxane; Temperature=304 K Spectrometer= Bruker WH-90
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Deuterium oxide
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent D2O
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent not reported
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent D2O
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent SEE COMMENT
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 H2O
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent H2O
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
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 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 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 PYRIDINE-D5
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 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 C5D5N
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 Unknown
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.
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 DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent H2O
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample O. Theander, Swedish Forest Products Research Laboratory, Stockholm, Sweden
Technique KBr WAFER
  • METHYL_BETA-D-GLUCOPYRANOSIDE
  • METHYL-BETA-D-GLUCOPYRANOSID
  • METHYL-O-BETA-D-GLUCOPYRANOSIDE
  • 1-O-METHYL-BETA-GLUCOPYRANOSIDE
  • METHYL-BETA-D-GLUCOSE,(PYRANOSID)
  • 1-O-METHYL-BETA-D-GLUCOSE
  • Methyl-b-d-glucopyranoside
  • Methyl β-D-galactopyranoside
  • Methyl .beta.-d-mannopyranoside
  • GLUCOPYRANOSIDE, METHYL, B-D-,
  • .BETA.-D-GLUCOPYRANOSIDE, METHYL
Title Journal or Book Year
Glycosylated Porphyra-334 and Palythine-Threonine from the Terrestrial Cyanobacterium Nostoc commune Marine Drugs 2013
A New Route to Carbohydrates Enriched with Oxygen Isotopes The Journal of Organic Chemistry 1998
A naphthalene glycoside from Cassia tora Phytochemistry 1995
Structure Elucidation of Three Triterpenoid Saponins from Alphitonia zizyphoides Using 2D Nmr Techniques Journal of Natural Products 1994
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
1H and 13C NMR data for 2‐O‐, 3‐O‐and 2,3‐di‐O‐glycosylated methyl α‐and β‐D‐galactopyranosides Magnetic Resonance in Chemistry 1993
NMR Spectroscopy in the structural elucidation of oligosaccharides and glycosides Phytochemistry 1992
New Stemodane Diterpenes from Stemodia maritima Journal of Natural Products 1992
Neue Triterpensaponine ausHelianthus annuus Planta Medica 1991
Saponins from Albizzia lucida Phytochemistry 1991
Terpenoid glycosides from Ophiopogon japonicus roots Phytochemistry 1990
A triterpene saponin from Cylicodiscus gabunensis Phytochemistry 1990
Methyl .ALPHA.-maltotrioside formed by transfer action of rice debranching enzyme. Agricultural and Biological Chemistry 1988
Studies on the constituents of asclepiadaceae plants. LV. The structures of three new glycosides, glaucoside-H, -I, and -J from the chinese drug "pai-ch'ien," Cynanchum glaucescens Hand-Mazz. Chemical and Pharmaceutical Bulletin 1983
Synthetic studies on cell surface glycans. Synthesis of 3-o-glycosyl-1,2-di-o-tetradecyl-sn-glycerol. Agricultural and Biological Chemistry 1982
Deuterium-induced differential isotope shift carbon-13 NMR. 1. Resonance reassignments of mono- and disaccharides Journal of the American Chemical Society 1979
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
Structures of stevia diterpene-glucosides : Application of 13C NMR Tetrahedron Letters 1976
Selective, reductive dechlorination of chlorodeoxy sugars. Structural determination of chlorodeoxy and deoxy sugars by 13C nuclear magnetic resonance spectroscopy Canadian Journal of Chemistry 1976
Application of Carbon-13 Nuclear Magnetic Resonance Spectroscopy to the Structural Determination of Chlorodeoxy Sugars Canadian Journal of Chemistry 1974
Configurational and conformational influences on the carbon-13 chemical shifts of some carbohydrates Canadian Journal of Chemistry 1970

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