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1-(2,3,4,5-TETRA-O-BENZOYL-BETA-D-GLUCOPYRANOSYL)-1H-BENZO-[D]-[1,2,3]-TRIAZOLE

Compound with spectra: 1 NMR

1-(2,3,4,5-TETRA-O-BENZOYL-BETA-D-GLUCOPYRANOSYL)-1H-BENZO-[D]-[1,2,3]-TRIAZOLE
SpectraBase Compound ID AKywUzP71YU
InChI InChI=1S/C40H31N3O9/c44-37(26-15-5-1-6-16-26)48-25-32-33(50-38(45)27-17-7-2-8-18-27)34(51-39(46)28-19-9-3-10-20-28)35(52-40(47)29-21-11-4-12-22-29)36(49-32)43-31-24-14-13-23-30(31)41-42-43/h1-24,32-36H,25H2/t32-,33-,34+,35-,36-/m0/s1
InChIKey NZFSLIWYRIGLDU-AGEXMYHWSA-N
Mol Weight 697.7 g/mol
Molecular Formula C40H31N3O9
Exact Mass 697.20603 g/mol
Enantiomer InChIKey NZFSLIWYRIGLDU-SQGINLDNSA-N

View Spectrum of 1-(2,3,4,5-TETRA-O-BENZOYL-BETA-D-GLUCOPYRANOSYL)-1H-BENZO-[D]-[1,2,3]-TRIAZOLE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
1-(2,3,4,5-TETRA-O-BENZOYL-ALPHA-D-MANNOPYRANOSYL)-1H-BENZO-[D]-[1,2,3]-TRIAZOLE
1-(2,3,4,5-TETRA-O-BENZOYL-BETA-D-MANNOPYRANOSYL)-1H-BENZO-[D]-[1,2,3]-TRIAZOLE
5-(1-HYDROXY-1-CARBOMETHOXYTRIFLUOROETHYL)-1-(TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSYL)INDOLE (DIASTEREOMER MIXTURE)]
9-[(1-(2,3,4,6-Tetra-o-acetyl-b-D-galactopyranosyl)-1H-1,2,3-triazol-4-yl)methyl]-3,6-dichloro-9H-carbazole
(2R,3R,4S,5R,6R)-2-(6-((E)-4-acetoxy-3-methylbut-2-enylamino)-9H-purin-9-yl)-6-(acetoxymethyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate
(2-R,3-R,4-R,5-R)-2-(BENZOYLOXYMETHYL)-5-(5-(HEXYLTHIO)-3-H-[1.2.3]-TRIAZOLO-[4.5-D]-PYRIMIDIN-3-YL)-TETRAHYDROFURAN-3,4-DIOL_DIBENZOATE
1-[2',3',4',6'-tetrakis(Acetyloxy)-.beta.-D-glucopyranosyl]-brassenin A
(2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-(6-(benzylamino)-7H-purin-7-yl)tetrahydro-2H-pyran-3,4,5-triyl triacetate
(2R,3R,4S,5R,6R)-2-(6-((E)-4-acetoxy-3-methylbut-2-enylamino)-7H-purin-7-yl)-6-(acetoxymethyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate
5,6-dimethyl-1-(D-glucopyranosyl)benzimidazole, tetraacetate
Title Journal or Book Year
'Click' Preparation of Carbohydrate 1-Benzotriazoles, 1,4-Disubstituted, and 1,4,5-Trisubstituted Triazoles and their Utility as Glycosyl Donors Australian Journal of Chemistry 2008
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