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1,2,6-TRIDEOXY-2,6-IMINO-L-GLYCERO-L-GLUCO-HEPTITOL

Compound with spectra: 1 NMR

1,2,6-TRIDEOXY-2,6-IMINO-L-GLYCERO-L-GLUCO-HEPTITOL
SpectraBase Compound ID 7ZWN4U3qn9w
InChI InChI=1S/C7H15NO4/c1-3-5(10)7(12)6(11)4(2-9)8-3/h3-12H,2H2,1H3/t3-,4+,5+,6+,7-/m0/s1
InChIKey ZEWFPWKROPWRKE-CJZRUXIPSA-N
Mol Weight 177.2 g/mol
Molecular Formula C7H15NO4
Exact Mass 177.100108 g/mol
Enantiomer InChIKey ZEWFPWKROPWRKE-PFCGLBSHSA-N

View Spectrum of 1,2,6-TRIDEOXY-2,6-IMINO-L-GLYCERO-L-GLUCO-HEPTITOL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
2,6,7-TRIDEOXY-2,6-IMINO-D-GLYCERO-L-GALACTO-HEPTITOL
1,2,6-TRIDEOXY-2,6-IMINO-L-GLYCERO-L-MANNO-HEPTITOL;ALPHA-HRJ
2,6,7-TRIDEOXY-2,6-IMINO-L-GLYCERO-L-GALACTO-HEPTITOL;BETA-HRJ
ALPHA-7-DEOXYHOMOMANNOJIRIMYCIN
ALPHA-7-DEOXYHOMONOJIRIMYCIN
2,6,7-TRIDEOXY-2,6-IMINO-D-GLYCERO-D-GLUCO-HEPTITOL
2-ALPHA,3-BETA,4-ALPHA-TRIHYDROXY-NORTROPANE
7-DEOXY-HOMO-DMDP;2,5-IMINO-2,5,7-TRIDEOXY-D-GLYCERO-D-MANNO-HEPTITOL
3-O-METHYL-1,5-DIDEOXY-1,5-IMINO-D-MANNITOL
3-O-METHYL-1,5-DIDEOXY-1,5-IMINO-D-GLUCITOL
Title Journal or Book Year
Synthesis of homorhamnojirimycins and related trihydroxypipecolic acid derivatives via divergent bicyclic amino lactone intermediates: Inhibition of naringinase (L-rhamnosidase) and dTDP-rhamnose biosynthesis Journal of the Chemical Society, Perkin Transactions 1 1999

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