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1-[BENZYL-(BUTYL-4'-O-OCTYL)]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE

Compound with spectra: 2 NMR

1-[BENZYL-(BUTYL-4'-O-OCTYL)]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE
SpectraBase Compound ID 5KOiL6xiq2W
InChI InChI=1S/2C46H61O8P/c2*1-2-3-4-5-6-19-30-48-31-20-21-32-52-55(47,53-36-42-28-17-10-18-29-42)38-44-46(51-35-41-26-15-9-16-27-41)45(50-34-40-24-13-8-14-25-40)43(54-44)37-49-33-39-22-11-7-12-23-39/h2*7-18,22-29,43-46H,2-6,19-21,30-38H2,1H3/t2*43-,44+,45-,46-,55?/m11/s1
InChIKey ODIOZURMQMRCKP-KUJXYNEPSA-N
Mol Weight 1545.9 g/mol
Molecular Formula C92H122O16P2
Exact Mass 1544.820812 g/mol
Enantiomer InChIKey ODIOZURMQMRCKP-DXNDUIGQSA-N

View Spectrum of 1-[BENZYL-(BUTYL-4'-O-OCTYL)]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of 1-[BENZYL-(BUTYL-4'-O-OCTYL)]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
1-[BENZYL-(BUTYL-4'-O-HEPTYL)]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE
1-[BENZYL-(BUTYL-4'-O-DODECYL)]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE
1-[BENZYL-(BUTYL-4'-O-HEXADECYL)]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE
1-[BENZYL-[(E)-2'-BUTENYL-4'-O-OCTYL]]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE
1-[BENZYL-[(E)-2'-BUTENYL-4'-O-NONYL]]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE
1-[BENZYL-[(E)-2'-BUTENYL-4'-O-HEPTYL]]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE
1-[BENZYL-[(E)-2'-BUTENYL-4'-O-DECYL]]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE
1-[BENZYL-[(E)-2'-BUTENYL-4'-O-DODECYL]]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE
DIMETHYL-2,6-ANHYDRO-1,7-DIDEOXY-4,5-DI-O-BENZYL-3-O-PARA-METHOXYBENZYL-L-GLYCERO-L-GALACTO-HEPTIT-1-YL-PHOSPHONATE;MAJOR-ISOMER
2,3,5-TRI-O-BENZYL-ALPHA-D-RIBOFURANOSYL-BENZYL-METHYLPHOSPHONATE
Title Journal or Book Year
Synthesis and Antituberculosis Activity of C-Phosphonate Analogues of Decaprenolphosphoarabinose, a Key Intermediate in the Biosynthesis of Mycobacterial Arabinogalactan and Lipoarabinomannan The Journal of Organic Chemistry 2002
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