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

Compound with spectra: 2 NMR

1-[BENZYL-(BUTYL-4'-O-HEPTYL)]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE
SpectraBase Compound ID LkxTZnF874
InChI InChI=1S/2C45H59O8P/c2*1-2-3-4-5-18-29-47-30-19-20-31-51-54(46,52-35-41-27-16-9-17-28-41)37-43-45(50-34-40-25-14-8-15-26-40)44(49-33-39-23-12-7-13-24-39)42(53-43)36-48-32-38-21-10-6-11-22-38/h2*6-17,21-28,42-45H,2-5,18-20,29-37H2,1H3/t2*42-,43+,44-,45-,54?/m11/s1
InChIKey FPJADAZPNUZVNR-VLSUHLHXSA-N
Mol Weight 1517.9 g/mol
Molecular Formula C90H118O16P2
Exact Mass 1516.789512 g/mol
Enantiomer InChIKey FPJADAZPNUZVNR-LXUYXXKGSA-N

View Spectrum of 1-[BENZYL-(BUTYL-4'-O-HEPTYL)]-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-HEPTYL)]-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-(ALLYLBENZYL)-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-MANNITYL-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-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-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
2,3,5-TRI-O-BENZYL-ALPHA-D-RIBOFURANOSYL-BENZYL-METHYLPHOSPHONATE
3-O-BENZYL-2-O-(2',3',4',6'-TETRA-O-BENZYL-BETA-D-GLUCOPYRANOSYL)-L-GLYCERALDEHYDE
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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