METHYL-7,8,9-TRI-O-ACETYL-2,6-ANHYDRO-3,5-DIDEOXY-4-O-METHYL-5-[(TRIFLUOROACETYL)-AMINO]-D-GLYCERO-D-TALO-NON-2-ENOATE
Compound with spectra: 1 NMR
![METHYL-7,8,9-TRI-O-ACETYL-2,6-ANHYDRO-3,5-DIDEOXY-4-O-METHYL-5-[(TRIFLUOROACETYL)-AMINO]-D-GLYCERO-D-TALO-NON-2-ENOATE](/api/compound/4GJh67feret.png?ph=true&h=300&w=458 "METHYL-7,8,9-TRI-O-ACETYL-2,6-ANHYDRO-3,5-DIDEOXY-4-O-METHYL-5-[(TRIFLUOROACETYL)-AMINO]-D-GLYCERO-D-TALO-NON-2-ENOATE")
| SpectraBase Compound ID | 4GJh67feret |
|---|---|
| InChI | InChI=1S/C19H24F3NO11/c1-8(24)31-7-13(32-9(2)25)15(33-10(3)26)16-14(23-18(28)19(20,21)22)11(29-4)6-12(34-16)17(27)30-5/h6,11,13-16H,7H2,1-5H3,(H,23,28)/t11-,13+,14-,15-,16-/m1/s1 |
| InChIKey | NXPNCIXPZAXNDV-DPZJBDQQSA-N |
| Mol Weight | 499.39 g/mol |
| Molecular Formula | C19H24F3NO11 |
| Exact Mass | 499.130145 g/mol |
| Enantiomer InChIKey | NXPNCIXPZAXNDV-TXUJKZCJSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
METHYL-7,8,9-TRI-O-ACETYL-2,6-ANHYDRO-3,5-DIDEOXY-4-O-ETHYL-5-[(TRIFLUOROACETYL)-AMINO]-D-GLYCERO-D-TALO-NON-2-ENOATE
METHYL-5-ACETAMIDO-4-C-ACETOXYMETHYL-7,8,9-TRI-O-ACETYL-2,6-ANHYDRO-3,4,5-TRIDEOXY-D-GLYCERO-BETA-D-GALACTO-NON-2-ENONATE
BENZYL-5-ACETAMIDO-4,7,8,9-TETRA-O-BENZYL-7-HYDROXY-3,5-DIDEOXY-D-GLYCERO-D-GALACTO-NON-2-ENOATE
METHYL-5-ACETAMIDO-4,7,8,9-TETRA-O-BENZYL-3,5-DIDEOXY-D-GLYCERO-D-GALACTO-NON-2-ENOATE
#8;METHYL-OXAZOLO-[5,4]-FUSED-7,8,9-TRI-O-ACETYL-2,3,4,5-TETRADEOXY-2,3-DIDEHYDRO-2,3-TRIDEOXY-4',5'-DIHYDRO-2'-METHYL-D-GLYCERO-D-TALO-NON-2-ENONATE
DIMETHYL-(4-ACETAMIDO-3,6,7,8-TETRA-O-ACETYL-2,4-DIDEOXY-D-GLYCERO-ALPHA-D-GALACTOOCTOPYRANOSYL)-PHOSPHONATE
DIMETHYL-7,8,9-TRI-O-ACETYL-3,4,5-TRIDEOXY-5-[(TRIFLUOROACETYL)-AMINO]-ALPHA-D-MANNO-NON-3-EN-2-ULOPYRANOSIDONATE
2-O-(3,4,6-TRI-O-ACETYL-2-N-ALLYLOXYCARBONYLAMINO-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-1,6-ANHYDRO-BETA-D-MANNOPYRANOSE
SEJLYQJBNHDCLD-KWXDATOUSA-N
SEJLYQJBNHDCLD-LYYGHALDSA-N
| Title | Journal or Book | Year |
|---|---|---|
| A Simple Synthetic Access to Differently 4‐Substituted Neu5Ac2en Glycals Combining Elements of Molecules with Anti‐Neuraminidase Activity | European Journal of Organic Chemistry | 2013 |