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HOVAGTYPODGVJG-XUUWZHRGSA-N

Compound with spectra: 32 NMR, 1 FTIR, and 1 MS (GC)

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

View Spectrum of HOVAGTYPODGVJG-XUUWZHRGSA-N

13C NMR Spectrum
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

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13C NMR Spectrum
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Solvent Deuterium oxide

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13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent D2O

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13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent not reported

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13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent D2O

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13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent SEE COMMENT

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent H2O

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent H2O

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown

View Spectrum of HOVAGTYPODGVJG-XUUWZHRGSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent PYRIDINE-D5

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown

View Spectrum of HOVAGTYPODGVJG-XUUWZHRGSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.

View Spectrum of HOVAGTYPODGVJG-XUUWZHRGSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown

View Spectrum of HOVAGTYPODGVJG-XUUWZHRGSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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17O NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent H2O

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FTIR Spectrum
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

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum CBD-20-SM5-5-3 (DOI: 10.1002/cbdv.202300332)
  • 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 .beta.-D-Glucopyranoside
  • Methyl β-D-galactopyranoside
  • Methyl .beta.-d-mannopyranoside
  • GLUCOPYRANOSIDE, METHYL, B-D-,
  • .BETA.-D-GLUCOPYRANOSIDE, METHYL
METHYL-ALPHA-D-GLUCOPYRANOSIDE-5-17O
METHYL alpha-D-ALTROPYRANOSIDE
METHYL-ALPHA-L-GLUCOPYRANOSIDE-6-17O
.ALPHA.-D-TALOPYRANOSIDE, METHYL-
1-O-METHYL-ALPHA-D-GLUCOPYRANOSIDE
.ALPHA.-D-IDOPYRANOSIDE, METHYL
METHYL-BETA-D-GULOSE,(PYRANOSID)
METHYL-BETA-D-ALLOSE,(PYRANOSID)
BETA-METHYL-D-MANNOSE
METHYL alpha-D-GALACTOPYRANOSIDE
METHYL-1-(18)-O-ALPHA-D-GLUCOPYRANOSIDE
METHYL alpha(D) IDOPYRANOSIDE
METHYL alpha-D-GLUCOPYRANOSIDE
METHYL-BETA-D-MANNOPYRANOSIDE;REFERENCE-10
METHYL-BETA-D-ALLOPYRANOSIDE-3-17O
Methyl .beta.-d-talopyranoside
METHYL-BETA-D-GLUGOPYRANOSIDE
D-Galactopyranoside, methyl-
METHYL-ALPHA-D-TALOSE,(PYRANOSID)
.BETA.-D-MANNOPYRANOSIDE, METHYL
METHYL alpha(D) GULOPYRANOSIDE
.BETA.-D-ALTROPYRANOSIDE, METHYL
METHYL-ALPHA-D-GLUGOPYRANOSIDE
METHYL-ALPHA-D-ALLOSE,(PYRANOSID)
.ALPHA.-D-ALTROPYRANOSIDE, METHYL
METHYL BETA-D-IDOPYRANOSIDE
alpha-D-METHYLMANNOPYRANOSIDE
METHYL-ALPHA-D-GLUCOPYRANOSIDE-3-17O
METHYL alpha(D) MANNOPYRANOSIDE
METHYL-BETA-D-ALTROSE,(PYRANOSID)
methyl .beta.-D-Glucopyranoside
METHYL alpha-D-GLUCOPYRANOSIDE
METHYL-ALPHA-D-MANNOPYRANOSIDE-2-17O
Methyl β-D-galactopyranoside
Methyl α-D-galactopyranoside monohydrate
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 and13C 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

This compound is available in the following databases:

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1-O-METHYL-ALPHA-D-GLUCOPYRANOSIDE
METHYL-BETA-D-GLUGOPYRANOSIDE
methyl .beta.-D-Glucopyranoside
Methyl β-D-galactopyranoside
BETA-METHYL-D-MANNOSE
METHYL-BETA-D-MANNOPYRANOSIDE;REFERENCE-10
Other Resources
Unknown Identification

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