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1-[BENZYL-[(E)-2'-BUTENYL-4'-O-HEXADECYL]]-3,4,6-TRI-O-BENZYL-2,5-ANHYDRO-D-GLUCITYL-PHOSPHONATE
SpectraBase Compound ID H5xU4PcPgVY
InChI InChI=1S/C54H75O8P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-27-38-56-39-28-29-40-60-63(55,61-44-50-36-25-18-26-37-50)46-52-54(59-43-49-34-23-17-24-35-49)53(58-42-48-32-21-16-22-33-48)51(62-52)45-57-41-47-30-19-15-20-31-47/h15-26,28-37,51-54H,2-14,27,38-46H2,1H3/b29-28+/t51-,52+,53-,54-,63?/m1/s1
InChIKey RICNYGIWSLILDJ-DAUIEYQNSA-N
Mol Weight 883.2 g/mol
Molecular Formula C54H75O8P
Exact Mass 882.519956 g/mol
Enantiomer InChIKey RICNYGIWSLILDJ-XEXGWDEWSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
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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