2-AMINO-2,5-DIDEOXY-4A(R)-HYDROXY-4A-CARBA-ALPHA-D-ARABINO-HEXOFURANOSE-HYDROCHLORIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | FJ50fui6ksF |
|---|---|
| InChI | InChI=1S/C7H15NO4.ClH/c8-4-5(10)3(1-2-9)6(11)7(4)12;/h3-7,9-12H,1-2,8H2;1H/t3-,4+,5-,6-,7-;/m1./s1 |
| InChIKey | UTWDMFACYYZTTF-PMDFCQFPSA-N |
| Mol Weight | 213.66 g/mol |
| Molecular Formula | C7H16ClNO4 |
| Exact Mass | 213.076786 g/mol |
| Parent InChIKey | XEUGZYIBPCLGCU-IECVIRLLSA-N |
| Enantiomer InChIKey | UTWDMFACYYZTTF-CZVAXXSJSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
(1R,2R,3R,4R,5R)-5-(Hydroxymethyl)-cyclohexane-1,2,3,4-tetraol
(1R,2R,3R,4R,5S)-5-(Hydroxymethyl)-cyclohexane-1,2,3,4-tetraol
(1S,2R,3R,4S,5S)-5-(Hydroxymethyl)-cyclohexane-1,2,3,4-tetraol
(1R,2R,3R,4S,5R)-5-(Hydroxymethyl)-cyclohexane-1,2,3,4-tetraol
BETA-HOMOGALACTONOJIRIMYCIN;2,6-DIDEOXY-2,6-IMINO-L-GLYCERO-L-GALACTO-HEPTITOL
ALPHA-3,4-DI-EPI-HOMONOJIRIMYCIN
2,6-DIDEOXY-2,6-IMINO-D-GLYCERO-L-GALACTO-HEPTITOL;ALPHA-HOMOGALACTONOJINIMYCIN
7-DEOXY-HOMO-DMDP;2,5-IMINO-2,5,7-TRIDEOXY-D-GLYCERO-D-MANNO-HEPTITOL
3-DEOXY-D-GLYCERO-D-GALACTO-2-NONULOSE
ALPHA-1-C-HYDROXYMETHYLFAGOMINE
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of carbasugars from aldonolactones. Part II. Preparation of polyhydroxy/aminocyclopentanes functionalised at all five ring carbons | Journal of the Chemical Society, Perkin Transactions 1 | 1999 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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