N-[9'-FLUORENYLMETHYL-OXYCARBONYL]-N-[3,4,6-TRI-O-ACETYL-1,5-ANHYDRO-2-DEOXY-GLUCITOL-2]-L-ASPARAGINE
Compound with spectra: 1 NMR
![N-[9'-FLUORENYLMETHYL-OXYCARBONYL]-N-[3,4,6-TRI-O-ACETYL-1,5-ANHYDRO-2-DEOXY-GLUCITOL-2]-L-ASPARAGINE](/api/compound/9vHrzgoSV.png?ph=true&h=300&w=458 "N-[9'-FLUORENYLMETHYL-OXYCARBONYL]-N-[3,4,6-TRI-O-ACETYL-1,5-ANHYDRO-2-DEOXY-GLUCITOL-2]-L-ASPARAGINE")
| SpectraBase Compound ID | 9vHrzgoSV |
|---|---|
| InChI | InChI=1S/C31H34N2O12/c1-16(34)41-15-26-29(45-18(3)36)28(44-17(2)35)25(14-42-26)32-27(37)12-24(30(38)39)33-31(40)43-13-23-21-10-6-4-8-19(21)20-9-5-7-11-22(20)23/h4-11,23-26,28-29H,12-15H2,1-3H3,(H,32,37)(H,33,40)(H,38,39)/t24-,25-,26+,28+,29+/m1/s1 |
| InChIKey | UBULHTIICIAFAC-XPNLVJAHSA-N |
| Mol Weight | 626.6 g/mol |
| Molecular Formula | C31H34N2O12 |
| Exact Mass | 626.211175 g/mol |
| Enantiomer InChIKey | UBULHTIICIAFAC-NCPANSIKSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
3-O-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSYL)-N(ALPHA)-9-(FLUORENYLMETHOXYCARBONYL)-L-SERINE
N(ALPHA)-(FLUOREN-9-YLMETHOXYCARBONYL)-C-(2,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOPYRANOSYL)-L-TYROSINE
N-(FLUOREN-9-YL-METHOXYCARBONYL)-L-CYSTEINE-[2-(2,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOPYRANOSYL-OXY)-ETHYL]-AMIDE
PLZJTETXMBPASH-CTARAAFWSA-N
2,3,4-TRI-O-BENZOYL-6-O-9-FLUORENYLMETHYLOXYCARBOXYL-ALPHA-D-GLUCOPYRANOSYL-BROMIDE
BENZYL-2,3,4-TRI-O-ACETYL-6-FLUORENYL-METHOXYCARBONYL-BETA-D-GLUCOPYRANOSIDE
Fmoc-Ala-Pro-D-Phe-Ser(TBS)-OBn
N-FMOC-MET-ALA-ILE-PRO-O-TBU
1,2,3,4-TETRA-O-ACETYL-6-O-FLUORENYLMETHOXYCARBONYL-BETA-D-MANNOPYRANOSIDE
1,2,3,4-TETRA-O-ACETYL-6-O-FLUORENYLMETHOXYCARBONYL-ALPHA-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 |