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

Compound with spectra: 2 NMR

1-[BENZYL-(BUTYL-4'-O-DECYL)]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE
SpectraBase Compound ID AQbVedq7vtF
InChI InChI=1S/2C48H65O8P/c2*1-2-3-4-5-6-7-8-21-32-50-33-22-23-34-54-57(49,55-38-44-30-19-12-20-31-44)40-46-48(53-37-43-28-17-11-18-29-43)47(52-36-42-26-15-10-16-27-42)45(56-46)39-51-35-41-24-13-9-14-25-41/h2*9-20,24-31,45-48H,2-8,21-23,32-40H2,1H3/t2*45-,46+,47-,48-,57?/m11/s1
InChIKey IYKVOMXQLMMYBO-KQMLYLQBSA-N
Mol Weight 1602.0 g/mol
Molecular Formula C96H130O16P2
Exact Mass 1600.883412 g/mol
Enantiomer InChIKey IYKVOMXQLMMYBO-HZXFTPHUSA-N

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