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ZYGZAHUNAGVTEC-HHKYUTTNSA-N

Compound with spectra: 5 NMR

ZYGZAHUNAGVTEC-HHKYUTTNSA-N
SpectraBase Compound ID 88qlwldsFdX
InChI InChI=1S/C11H22O6/c1-12-6-7-8(13-2)9(14-3)10(15-4)11(16-5)17-7/h7-11H,6H2,1-5H3/t7-,8-,9+,10-,11-/m0/s1
InChIKey ZYGZAHUNAGVTEC-HHKYUTTNSA-N
Mol Weight 250.29 g/mol
Molecular Formula C11H22O6
Exact Mass 250.141638 g/mol
Enantiomer InChIKey ZYGZAHUNAGVTEC-KAMPLNKDSA-N

View Spectrum of ZYGZAHUNAGVTEC-HHKYUTTNSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of ZYGZAHUNAGVTEC-HHKYUTTNSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of ZYGZAHUNAGVTEC-HHKYUTTNSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CH2Cl2-D2

View Spectrum of ZYGZAHUNAGVTEC-HHKYUTTNSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CH2Cl2-D2*5ME3SIOTF

View Spectrum of ZYGZAHUNAGVTEC-HHKYUTTNSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CH3CN-D3
  • METHYL-2,3,4,6-TETRA-O-METHYL-BETA-D-GLUCOPYRANOSIDE
ZYGZAHUNAGVTEC-UNQZSWDGSA-N
a methyl glycoside of a tetra - O - methyl - hexose
(2R,3R,4S,5S,6R)-2,3,4,5-tetramethoxy-6-(methoxymethyl)oxane
Methyl 2,3,4,6-tetra-O-trideuteriomethyl-.beta.,d-galactoside
ZYGZAHUNAGVTEC-FBDQPXRJSA-N
(2R,3S,4S,5R,6R)-2,3,4,5-tetramethoxy-6-(methoxymethyl)oxane
ZYGZAHUNAGVTEC-GEVSDDDWSA-N
METHYL 2,3,4,6-TETRA-O-METHYL-ALPHA-D-MANNOPYRANOSIDE
ZYGZAHUNAGVTEC-QUARPLMYSA-N
Methyl-3,6-anhydro-2,4-di-O-methyl-.alpha.-D-glucopyranoside
2-BROMOMETHYL-3,4,5,6-TETRAMETHOXYTETRAHYDROPYRAN
Methyl 6-bromo-6-deoxy-2,3,4-tri-O-methylhexopyranoside
1,6-Anhydro-2,3,4-tri-O-methylgalactose
Title Journal or Book Year
Mechanism of anomerization of permethylated methyl d-glycopyranosides by trimethylsilyl trifluoromethanesulfonate Carbohydrate Research 1998
Action of Grignard reagents on hexuronic esters and attempted dehydration of tertiary alcohols to give hex-5-enopyranosides Canadian Journal of Chemistry 1976

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