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#5.2HCL;(+/-)-(1RS,2RS,3SR,4SR,5SR)-5-EXO-BENZYLAMINO-7-AZABICYCLO-[2.2.1]-HEPTANE-2,3-EXO-DIOL-DIHYDROCHLORIDE;(1RS,2RS,3SR,4SR,5SR)-5-BENZYLAMMONIO)-2

Compound with spectra: 1 NMR

#5.2HCL;(+/-)-(1RS,2RS,3SR,4SR,5SR)-5-EXO-BENZYLAMINO-7-AZABICYCLO-[2.2.1]-HEPTANE-2,3-EXO-DIOL-DIHYDROCHLORIDE;(1RS,2RS,3SR,4SR,5SR)-5-BENZYLAMMONIO)-2
SpectraBase Compound ID 8g2mszpee3a
InChI InChI=1S/C13H18N2O2.2ClH/c16-12-10-6-9(11(15-10)13(12)17)14-7-8-4-2-1-3-5-8;;/h1-5,9-17H,6-7H2;2*1H/t9-,10-,11+,12+,13-;;/m0../s1
InChIKey UUJDYHHPVNLFER-UZBUBUSJSA-N
Mol Weight 307.22 g/mol
Molecular Formula C13H20Cl2N2O2
Exact Mass 306.090183 g/mol
Parent InChIKey WJWFRPZGVXZFRC-YYHQMBLXSA-N
Enantiomer InChIKey UUJDYHHPVNLFER-NBIKFQCXSA-N

View Spectrum of #5.2HCL;(+/-)-(1RS,2RS,3SR,4SR,5SR)-5-EXO-BENZYLAMINO-7-AZABICYCLO-[2.2.1]-HEPTANE-2,3-EXO-DIOL-DIHYDROCHLORIDE;(1RS,2RS,3SR,4SR,5SR)-5-BENZYLAMMONIO)-2

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
#7.2HCL;(+/-)-(1RS,2RS,3SR,4SR,5RS)-5-ENDO-BENZYLAMINO-7-AZABICYCLO-[2.2.1]-HEPTANE-2,3-EXO-DIOL-DIHYDROCHLORIDE;(1RS,2RS,3SR,4SR,5RS)-5-BENZYLAMMONIO)-
N-BUTYL-2,6,7-TRIDEOXY-2,6-IMINO-L-GLYCERO-L-TALO-HEPTONAMIDE
(2S,3R,4R,5R)-2-(AMINOMETHYL)-1-BENZYL-3,4,5-TRIHYDROXY-PIPERIDINE
N-(BENZYL)-BETA-D-GALACTOPYRANOSYLAMINE
1-o-Acetyl-3,4-dideoxy-5,6-o-(1'-methylethylidene)-4-[(phenylmethyl)amino]-D-lyxo-hexitol
U-47700-M (N,N-bis-demethyl-HO-) MS2
1-Ethynyl-2-(benzylamino)cyclohaxane
N-(4-CHLOROBENZYL)-BETA-D-GALACTOPYRANOSYLAMINE
(1R*,2S*)-N-Benzyl-2-[1S*-hydroxy-2-(phenylthio)-2-propenyl]cyclopentamine
N-BENZYL-1,5-DIDEOXY-1,5-IMINO-D-MANNITOL
Title Journal or Book Year
Synthesis of Enantiomerically Pure 1,2-Diamine Derivatives of 7-Azabicyclo[2.2.1]heptane. New Leads as Glycosidase Inhibitors and Rigid Scaffolds for the Preparation of Peptide Analogues The Journal of Organic Chemistry 2003
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