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Methyl β-D-galactopyranoside
SpectraBase Compound ID Esr87W0pNJ6
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-VOQCIKJUSA-N
Mol Weight 194.18 g/mol
Molecular Formula C7H14O6
Exact Mass 194.079038 g/mol
Enantiomer InChIKey HOVAGTYPODGVJG-XUVCUMPTSA-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 not reported
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent D2O
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 D2O
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 D2O
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 D2O
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 CD3OD
Copyright Copyright © 2021-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Co. LLC.
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number 296392
Solvent D2O
Copyright Copyright © 2014-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample TCI Chemicals India Pvt. Ltd.
Source of Spectrum Bio-Rad Laboratories
Catalog Number M1035
Copyright Copyright © 2016-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample TCI Chemicals India Pvt. Ltd.
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number M1035
Technique KBr1
Copyright Copyright © 2015-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample TCI Chemicals India Pvt. Ltd.
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number M1035
Copyright Copyright © 2018-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2018-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich
Catalog Number 296392
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum CBD-20-SM5-5-6 (DOI: 10.1002/cbdv.202300332)
Copyright Copyright © 2021-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Co. LLC.
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number 296392
Solvent D2O
  • (2R,3R,4S,5R,6R)-2-(Hydroxymethyl)-6-methoxyoxane-3,4,5-triol
  • Methyl β-D-galactoside
  • METHYL-BETA-D-GALACTOPYRANOSID
  • ME-BETA-GAL;O-METHYL-BETA-D-GALACOPYRANOSIDE
  • METHYL-BETA-D-GALAKTOSE,(PYRANOSID)
  • G-ME;1-O-BETA-METHYL-GALACTOPYRANOSIDE
  • methyl .beta.-D-thiogalactoside
  • .BETA.-D-GALACTOPYRANOSIDE, METHYL
Title Journal or Book Year
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
Transfer Reaction Catalyzed by Exo-.BETA.-1,4-galactanase from Bacillus subtilis. Agricultural and Biological Chemistry 1991
Structures of KS-501 and KS-502, the new inhibitors of Ca2+ and calmodulin-dependent cyclic nucleotide phosphodiesterase. The Journal of Antibiotics 1990
Formation of transfer products from soybean arabinogalactan and glycerol by galactanase from Penicillium citrinum. Agricultural and Biological Chemistry 1988
The conformations of oligosaccharides related to the ABH and Lewis human blood group determinants Canadian Journal of Chemistry 1980
Deuterium-induced differential isotope shift carbon-13 NMR. 1. Resonance reassignments of mono- and disaccharides Journal of the American Chemical Society 1979
The influence of methylation on 13C chemical shifts of galactose derivatives Tetrahedron 1973
Unknown Identification

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