1-[N-(6-HYDROXYHEXYL)-AMINO]-1-N,2-O-CARBONYL-1-DEOXY-BETA-D-GALACTO-HEPT-2-ULO-PYRANOSIDE
Compound with spectra: 1 NMR
![1-[N-(6-HYDROXYHEXYL)-AMINO]-1-N,2-O-CARBONYL-1-DEOXY-BETA-D-GALACTO-HEPT-2-ULO-PYRANOSIDE](/api/compound/Bp9rT1id2xa.png?ph=true&h=300&w=458 "1-[N-(6-HYDROXYHEXYL)-AMINO]-1-N,2-O-CARBONYL-1-DEOXY-BETA-D-GALACTO-HEPT-2-ULO-PYRANOSIDE")
| SpectraBase Compound ID | Bp9rT1id2xa |
|---|---|
| InChI | InChI=1S/C14H25NO8/c16-6-4-2-1-3-5-15-8-14(23-13(15)21)12(20)11(19)10(18)9(7-17)22-14/h9-12,16-20H,1-8H2/t9-,10+,11+,12-,14+/m1/s1 |
| InChIKey | UHDNGMRGNASQBU-LARJDALCSA-N |
| Mol Weight | 335.35 g/mol |
| Molecular Formula | C14H25NO8 |
| Exact Mass | 335.158017 g/mol |
| Enantiomer InChIKey | UHDNGMRGNASQBU-ILOGHGLZSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
1-[N-(5-METHOXYCARBONYL-PENTYL)-AMINO]-1-N,2-O-CARBONYL-1-DEOXY-BETA-D-GALACTO-HEPT-2-ULO-PYRANOSIDE
1-[N-[5-(METHOXYCARBONYL)-PENTYL]-AMINO]-1-N,2-O-CARBONYL-1-DEOXY-BETA-D-MANNO-HEPT-2-ULO-PYRANOSIDE
1-(N,N-DIBENZYLAMINO)-3-ACETAMIDO-1,3-DIDEOXY-ALPHA-D-GLUCO-HEPT-2-ULO-PYRANOSIDE/FURANOSIDE;MIXTURE
O-BETA-D-FRUCTOFURANOSYL-(2->1)-O-[BETA-D-GLUCOPYRANOSYL-(1->3)]-BETA-D-GLUCOPYRANOSIDE;3(G)-BETA-D-GLUCOPYRANOSYL-BETA,BETA-ISOSUCROSE
#7;3-AZIDOPROPYL-BETA-D-GALACTOPYRANOSYL-(1->3)-2-DEOXY-2-ACETAMIDO-BETA-D-GLUCOPYRANOSYL-(1->3)-2-DEOXY-2-ACETAMIDO-ALPHA-D-GALACTOPYRANOSIDE-HYDROCHLORIDE
2-O-(4-PHENYLBUTYRYL)-SUCROSE
SIBIRICOSE-A2;6-O-3,4,5-TRIMETHOXYCINNAMOYL-SUCROSE
BENZYL-2-ALPHA-O-METHYL-5-N-ACETYL-NEURAMINATE
3-BENZYLOXYCARBONYLAMINOPROPYL-2-DEOXY-2-(1-DEOXY-1-TERT.-BUTOXYCARBONYLAMINOMETHYL-BETA-D-GALACTOHEXOPYRANOSYLURONAMIDE)-BETA-D-GLUCOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| The Amadori rearrangement as glycoconjugation method: Synthesis of non-natural C-glycosyl type glycoconjugates | Beilstein Journal of Organic Chemistry | 2012 |