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2,5-DIDEOXY-2,5-IMINO-D-(2D)-MANNITOL

Compound with spectra: 1 NMR

2,5-DIDEOXY-2,5-IMINO-D-(2D)-MANNITOL
SpectraBase Compound ID EQ6LcuQVShU
InChI InChI=1S/C6H13NO4/c8-1-3-5(10)6(11)4(2-9)7-3/h3-11H,1-2H2/t3-,4-,5-,6-/m1/s1/i3D
InChIKey PFYHYHZGDNWFIF-JNHZOBAGSA-N
Mol Weight 164.18 g/mol
Molecular Formula C6H122HNO4
Exact Mass 164.090735 g/mol
Enantiomer InChIKey PFYHYHZGDNWFIF-GLBDTLMASA-N

View Spectrum of 2,5-DIDEOXY-2,5-IMINO-D-(2D)-MANNITOL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
2,5-DIDEOXY-2,5-IMINO-D-ALTRITOL
2,5-Dihydroxymethyl-3,4-dihydroxy-pyrrolidine
2R,5R-BIS-(HYDROXYMETHYL)-3R,4R-DIHYDROXYPYRROLIDINE
2,5-ANHYDRO-2,5-IMINO-D-GLUCITOL
2,5-DIDEOXY-2,5-IMINO-D-GALACTITOL
2,5-DIDEOXY-2,5-IMINO-L-ALTRITOL
DMDP;(2R,3R,4R,5R)-2,5-BIS-(HYDROXYMETHYL)-3,4-DIHYDROXY-PYRROLIDINE;1,6-13C-LABELED
2,5-DIDEOXY-2,5-IMINO-D-(5D)-GLUCITOL
2R,5R-BIS-(HYDROXYMETHYL)-3R,4R-DIHYDROXYPYRROLIDINE
DMDP;(2R,3R,4R,5R)-2,5-BIS-(HYDROXYMETHYL)-3,4-DIHYDROXY-PYRROLIDINE;1,6-13C-LABELED
6-DEOXY-6-C-(2,5-DIHYDROXY-HEXYL)-(2R,5R)-BIS-HYDROXY-METHYL-(3R,4R)-DIHYDROXY-PYRROLIDINE
(2R,3R,4S,5R,6R)-2-methylolazepane-3,4,5,6-tetrol
GALACTOSTATIN-LACTAM;5-AMINO-5-DEOXY-GALACTONIC-DELTA-LACTAM
1-DEOXYNOJIRIMYCIN-6-PHOSPHATE
BXEBAGZZVNWTME-UHFFFAOYSA-N
6-THIO-BETA-L-TAGATOPYRANOSE
1S,2R,6R,7S-1,2,6,7-Tetrahydroxy-pyrrolizidinium cation
1S,2R,6R,7S-1,2,6,7-Tetrahydroxy-pyrrolizidine
N,N'-(2,3,5,6-TETRAHYDROXY-1,4-CYCLOHEXYLENE)BISACETAMIDE
Title Journal or Book Year
Synthesis of regio- and stereospecifically C-deuterated derivatives of glycosidase inhibitors 1-deoxymannonojirimycin and 2,5-dideoxy-2,5-imino-d-mannitol by intramolecular reductive amination employing deuterium gas1Dedicated to Professor Herfried Griengl on the occasion of his 60th birthday.1 Carbohydrate Research 1998

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