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(-)-TRANS-2-FLUOROCYCLOHEXYL-N-[PARA-(4'-METHYL-BETA-D-GLUCOPYRANOACETYL)]-PHENYLCARBAMATE

Compound with spectra: 2 NMR

(-)-TRANS-2-FLUOROCYCLOHEXYL-N-[PARA-(4'-METHYL-BETA-D-GLUCOPYRANOACETYL)]-PHENYLCARBAMATE
SpectraBase Compound ID LZI4c2nFJ6K
InChI InChI=1S/C26H34FNO11/c1-14(29)34-13-21-22(33-4)23(35-15(2)30)24(36-16(3)31)25(38-21)37-18-11-9-17(10-12-18)28-26(32)39-20-8-6-5-7-19(20)27/h9-12,19-25H,5-8,13H2,1-4H3,(H,28,32)/t19-,20-,21+,22+,23-,24+,25+/m0/s1
InChIKey JRHVWTKLTKKQHU-CQYMSPLPSA-N
Mol Weight 555.6 g/mol
Molecular Formula C26H34FNO11
Exact Mass 555.211589 g/mol
Enantiomer InChIKey JRHVWTKLTKKQHU-MVKKGCRCSA-N

View Spectrum of (-)-TRANS-2-FLUOROCYCLOHEXYL-N-[PARA-(4'-METHYL-BETA-D-GLUCOPYRANOACETYL)]-PHENYLCARBAMATE

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (-)-TRANS-2-FLUOROCYCLOHEXYL-N-[PARA-(4'-METHYL-BETA-D-GLUCOPYRANOACETYL)]-PHENYLCARBAMATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
4-(4'-N,N-DIDODECYLAMINOPHENYLAZO)-PHENYL-2,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOPYRANOSIDE
1-O-[ALPHA-(META-TRIFLUOROMETHYLPHENYLIMINO)-4-BENZYL]-2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSIDE
4-(4'-N,N-DIDODECYLAMINOPHENYLAZO)-PHENYL-2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSIDE
4-(4'-N,N-DIDODECYLAMINOPHENYLAZO)-PHENYL-2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSIDE
DIGLUCOPYRANOSYL-BIS-DEMETHOXYCURCUMIN-OCTAACETATE
MONOGLUCOPYRANOSYL-BIS-DEMETHOXYCURCUMIN-TETRAACETATE
2,4,6-TRIHYDROXYBENZOIC-ACID-4-O-2',3',4',6'-TETRAACETYLGLUCOSIDE
.beta.-D-Glucopyranoside, 2-methylphenyl, tetraacetate
3,5-Bis-(2,3,4,6-tetra-O-acetyl-b-d-glucopyranosyl)-benzaldehyde
2-(beta-D-glucopyranosyloxy)-4-picoline, tetraacetate (ester)
Title Journal or Book Year
Selectivity of Biohydroxylation with Beauveria bassiana of trans-2-Fluorocycloalkyl N-Phenylcarbamates The Journal of Organic Chemistry 2002
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