N-BENZYL-OXYCARBONYL-N-[3,4,6-TRI-O-ACETYL-1,5-ANHYDRO-2-DEOXY-GLUCITOL-2]-2-ASPARAGINE-BENZYLESTER
Compound with spectra: 1 NMR
![N-BENZYL-OXYCARBONYL-N-[3,4,6-TRI-O-ACETYL-1,5-ANHYDRO-2-DEOXY-GLUCITOL-2]-2-ASPARAGINE-BENZYLESTER](/api/compound/1c0nLrQ0kF4.png?ph=true&h=300&w=458 "N-BENZYL-OXYCARBONYL-N-[3,4,6-TRI-O-ACETYL-1,5-ANHYDRO-2-DEOXY-GLUCITOL-2]-2-ASPARAGINE-BENZYLESTER")
| SpectraBase Compound ID | 1c0nLrQ0kF4 |
|---|---|
| InChI | InChI=1S/C31H36N2O12/c1-19(34)40-18-26-29(45-21(3)36)28(44-20(2)35)25(17-41-26)32-27(37)14-24(30(38)42-15-22-10-6-4-7-11-22)33-31(39)43-16-23-12-8-5-9-13-23/h4-13,24-26,28-29H,14-18H2,1-3H3,(H,32,37)(H,33,39)/t24-,25+,26-,28-,29-/m0/s1 |
| InChIKey | ZIEUQEJFIBBCQL-GCNJZUOMSA-N |
| Mol Weight | 628.6 g/mol |
| Molecular Formula | C31H36N2O12 |
| Exact Mass | 628.226825 g/mol |
| Enantiomer InChIKey | ZIEUQEJFIBBCQL-IFJBLKETSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1-AZIDO-3-OXOPENTYL-2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE
1-HEXYL-2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE
PENTYL-4'-ENYL-3,4,6-TRI-O-ACETYL-2-ACETYLAMINO-2-DEOXY-BETA-D-GLUCOSIDE
BUT-3'-ENYL-3,4,6-TRI-O-ACETYL-2-ACETYLAMINO-2-DEOXY-BETA-D-GLUCOSIDE
Allyl-3,4,6-tri-O-acetyl-2-acetylamino-2-deoxy-b-d-glucopyranoside
ALLYL-2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-ALPHA-D-GLUCOPYRANOSIDE
3-(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-ALPHA-D-GLUCOPYRANOSYL)-1-PROPENE
3-(2-ACETAMIDO-3,4,5-TRI-O-ACETYL-2-DEOXY-ALPHA-D-GALCTOPYRANOSYL)-1-PROPENE
4,6,7,8,9-PENTA-O-ACETYL-5-ACETYLAMINO-3,5-DIDEOXY-D-GLYCERO-D-GALACTO-2-NONULOSE
METHYL-3,4,6-TRI-O-ACETYL-2-DEOXY-2-ETHYLUREIDO-BETA-D-GLUCOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of an N-glucoasparagine analog as a building block for a V3-loop glycopeptide from GP120 of HIV-I | Carbohydrate Research | 1998 |