ETHYL-METHYL-7,8,9-TRI-O-ACETYL-3,4,5-TRIDEOXY-2-THIO-5-[(TRIFLUOROACETYL)-AMINO]-ALPHA-D-MANNO-NON-3-EN-2-ULOPYRASIDONATE
Compound with spectra: 1 NMR
![ETHYL-METHYL-7,8,9-TRI-O-ACETYL-3,4,5-TRIDEOXY-2-THIO-5-[(TRIFLUOROACETYL)-AMINO]-ALPHA-D-MANNO-NON-3-EN-2-ULOPYRASIDONATE](/api/compound/8CcDETdQWPj.png?ph=true&h=300&w=458 "ETHYL-METHYL-7,8,9-TRI-O-ACETYL-3,4,5-TRIDEOXY-2-THIO-5-[(TRIFLUOROACETYL)-AMINO]-ALPHA-D-MANNO-NON-3-EN-2-ULOPYRASIDONATE")
| SpectraBase Compound ID | 8CcDETdQWPj |
|---|---|
| InChI | InChI=1S/C20H26F3NO10S/c1-6-35-19(18(29)30-5)8-7-13(24-17(28)20(21,22)23)15(34-19)16(33-12(4)27)14(32-11(3)26)9-31-10(2)25/h7-8,13-16H,6,9H2,1-5H3,(H,24,28)/t13-,14+,15-,16-,19+/m1/s1 |
| InChIKey | MGWSNBRRDZWIPX-INJPQVFBSA-N |
| Mol Weight | 529.48 g/mol |
| Molecular Formula | C20H26F3NO10S |
| Exact Mass | 529.122952 g/mol |
| Enantiomer InChIKey | MGWSNBRRDZWIPX-ZHEXZJMTSA-N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
SEJLYQJBNHDCLD-KWXDATOUSA-N
SEJLYQJBNHDCLD-LYYGHALDSA-N
METHYL-2,6-ANHYDRO-4-PROPOXYCARBONYLAMIDO-5-(2,2,2-TRIFLUOROACETAMIDO)-7,8,9-TRI-O-ACETYL-3,4,5-TRIDEOXY-D-GLYCERO-D-TALO-NON-2-ENONATE
METHYL-7,8,9-TRI-O-ACETYL-2,6-ANHYDRO-3,5-DIDEOXY-4-S-PHENYL-4-THIO-5-[(TRIFLUOROACETYL)-AMINO]-D-GLYCERO-D-GALACTO-NON-2-ENONATE
METHYL-7,8,9-TRI-O-ACETYL-2,6-ANHYDRO-3,5-DIDEOXY-4-O-(4-METHYLPHENYL)-5-[(TRIFLUOROACETYL)-AMINO]-D-GLYCERO-D-GALACTO-NON-2-ENOATE
METHYL-4-ACETAMIDO-2,6-ANHYDRO-5-(2,2,2-TRIFLUOROACETAMIDO)-7,8,9-TRI-O-ACETYL-3,4,5-TRIDEOXY-D-GLYCERO-D-GALACTO-NON-2-ENONATE
METHYL-4-ACETAMIDO-2,6-ANHYDRO-5-(2,2,2-TRIFLUOROACETAMIDO)-7,8,9-TRI-O-ACETYL-3,4,5-TRIDEOXY-D-GLYCERO-D-TALO-NON-2-ENONATE
METHYL-7,8,9-TRI-O-ACETYL-2,6-ANHYDRO-3,5-DIDEOXY-4-S-OCTYL-4-THIO-5-[(TRIFLUOROACETYL)-AMINO]-D-GLYCERO-D-GALACTO-NON-2-ENONATE
METHYL-4-ACETAMIDO-7,8,9-TRI-O-ACETYL-2,6-ANHYDRO-5-(BENZYLOXYACETAMIDO)-3,4,5-TRIDEOXY-D-GLYCERO-D-TALO-NON-2-ENONATE
| 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 |