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METHYL-TETRA-O-ACETYL-ALPHA-D-GLUCOPYRANOSIDE
SpectraBase Compound ID DVWSssAtYW1
InChI InChI=1S/C15H22O10/c1-7(16)21-6-11-12(22-8(2)17)13(23-9(3)18)14(24-10(4)19)15(20-5)25-11/h11-15H,6H2,1-5H3/t11-,12-,13+,14-,15+/m0/s1
InChIKey UYWUMFGDPBMNCA-SBJFKYEJSA-N
Mol Weight 362.33 g/mol
Molecular Formula C15H22O10
Exact Mass 362.121297 g/mol
Enantiomer InChIKey UYWUMFGDPBMNCA-QMIVOQANSA-N
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 Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • PERACETYLATED-ALPHA-METHYL-GLUCOPYRANOSIDE
  • UYWUMFGDPBMNCA-SBJFKYEJSA-N
  • 2,3,4,6-TETRA-O-ACETYL-METHYL-ALPHA-D-GLUCOPYRANOSIDE
Title Journal or Book Year
A Simple Preparation of 2,3,4,6-Tetra-O-acyl-Gluco-, Galacto- and Mannopyranoses and Relevant Theoretical Study Molecules 2010
Probing the Transition States of Four Glucoside Hydrolyses with 13C Kinetic Isotope Effects Measured at Natural Abundance by NMR Spectroscopy Journal of the American Chemical Society 2004
Ellagic compounds from Diplopanax stachyanthus 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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