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

Compound with spectra: 2 NMR

1-[BENZYL-(BUTYL-4'-O-NONYL)]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE
SpectraBase Compound ID 5GdOTbYi8YL
InChI InChI=1S/2C47H63O8P/c2*1-2-3-4-5-6-7-20-31-49-32-21-22-33-53-56(48,54-37-43-29-18-11-19-30-43)39-45-47(52-36-42-27-16-10-17-28-42)46(51-35-41-25-14-9-15-26-41)44(55-45)38-50-34-40-23-12-8-13-24-40/h2*8-19,23-30,44-47H,2-7,20-22,31-39H2,1H3/t2*44-,45+,46-,47-,56?/m11/s1
InChIKey IESYKDLPEJZFFZ-NETBXDIDSA-N
Mol Weight 1574.0 g/mol
Molecular Formula C94H126O16P2
Exact Mass 1572.852112 g/mol
Enantiomer InChIKey IESYKDLPEJZFFZ-KUQKFWPLSA-N

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