1-[N-(5-METHOXYCARBONYL-PENTYL)-AMINO]-1-N,2-O-CARBONYL-1-DEOXY-BETA-D-GALACTO-HEPT-2-ULO-PYRANOSIDE
Compound with spectra: 1 NMR
![1-[N-(5-METHOXYCARBONYL-PENTYL)-AMINO]-1-N,2-O-CARBONYL-1-DEOXY-BETA-D-GALACTO-HEPT-2-ULO-PYRANOSIDE](/api/compound/CAJeilHoxiP.png?ph=true&h=300&w=458 "1-[N-(5-METHOXYCARBONYL-PENTYL)-AMINO]-1-N,2-O-CARBONYL-1-DEOXY-BETA-D-GALACTO-HEPT-2-ULO-PYRANOSIDE")
| SpectraBase Compound ID | CAJeilHoxiP |
|---|---|
| InChI | InChI=1S/C15H25NO9/c1-23-10(18)5-3-2-4-6-16-8-15(25-14(16)22)13(21)12(20)11(19)9(7-17)24-15/h9,11-13,17,19-21H,2-8H2,1H3/t9-,11+,12+,13-,15+/m1/s1 |
| InChIKey | BOOVCQMBCSSEOG-XTYGHYOUSA-N |
| Mol Weight | 363.36 g/mol |
| Molecular Formula | C15H25NO9 |
| Exact Mass | 363.152931 g/mol |
| Enantiomer InChIKey | BOOVCQMBCSSEOG-UHNMOKONSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
#30;1-[N-(6-HYDROXYHEXYL)-AMINO]-1-N,2-O-CARBONYL-1-DEOXY-BETA-D-MANNO-HEPT-2-ULO-PYRANOSIDE;1-N-(HYDROXYHEXYL)-AMINO-BETA-D-MANNO-1-N,2-O-CARBAMATE
1-[N-(6-HYDROXYHEXYL)-AMINO]-1-N,2-O-CARBONYL-1-DEOXY-BETA-D-GALACTO-HEPT-2-ULO-PYRANOSIDE
1-(N,N-DIBENZYLAMINO)-3-ACETAMIDO-1,3-DIDEOXY-ALPHA-D-GLUCO-HEPT-2-ULO-PYRANOSIDE/FURANOSIDE;MIXTURE
2-O-(4-PHENYLBUTYRYL)-SUCROSE
SIBIRICOSE-A2;6-O-3,4,5-TRIMETHOXYCINNAMOYL-SUCROSE
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
#8A;QUAMOCLINIC-ACID-C;(3S,11S)-IPUROLIC-ACID-11-O-BETA-D-QUINOVOPYRANOSYL-(1->2)-O-BETA-D-GLUCOPYRANOSYL-(1->3)-[O-BETA-D-QUINOVOPYRANOSYL-(1->4)]-O-ALPHA-L-R
#9A;QUAMOCLINIC-ACID-D;(3S,11S)-IPUROLIC-ACID-11-O-BETA-D-QUINOVOPYRANOSYL-(1->2)-O-BETA-D-GLUCOPYRANOSYL-(1->3)-[O-BETA-D-FUCOPYRANOSYL-(1->4)]-O-ALPHA-L-RHAM
| 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 |