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6'-O-[(2,2,2-TRICHLOROETHOXY)-CARBONYL]-ACETYL_GINSENOSIDE_RG1

Compound with spectra: 1 NMR

6'-O-[(2,2,2-TRICHLOROETHOXY)-CARBONYL]-ACETYL_GINSENOSIDE_RG1
SpectraBase Compound ID E8oU4vJHiPs
InChI InChI=1S/C47H75Cl3O17/c1-22(2)10-9-13-46(8,67-41-38(61)35(58)33(56)26(19-51)65-41)23-11-15-44(6)32(23)24(52)16-28-43(5)14-12-29(53)42(3,4)39(43)25(18-45(28,44)7)64-40-37(60)36(59)34(57)27(66-40)20-62-30(54)17-31(55)63-21-47(48,49)50/h10,23-29,32-41,51-53,56-61H,9,11-21H2,1-8H3/t23-,24+,25-,26+,27+,28?,29-,32-,33+,34+,35-,36-,37+,38+,39?,40+,41-,43+,44+,45+,46-/m0/s1
InChIKey CZIUBDCYMNIYJL-GTZUFSNTSA-N
Mol Weight 1018.5 g/mol
Molecular Formula C47H75Cl3O17
Exact Mass 1016.406984 g/mol
Enantiomer InChIKey CZIUBDCYMNIYJL-RLGWLBBOSA-N

View Spectrum of 6'-O-[(2,2,2-TRICHLOROETHOXY)-CARBONYL]-ACETYL_GINSENOSIDE_RG1

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6:D2O
Title Journal or Book Year
Regioselective Enzyme-Mediated Acylation of Polyhydroxy Natural Compounds. A Remarkable, Highly Efficient Preparation of 6'-Acetyl and 6'-O-Carboxyacetyl Ginsenoside Rg1 The Journal of Organic Chemistry 1995
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