CIS-3-METHYL-TRANS-2-(4-MORPHOLINO)-CYClOHEXANOL
Compound with spectra: 1 NMR
| SpectraBase Compound ID | BLGDeAesam0 |
|---|---|
| InChI | InChI=1S/C11H21NO2/c1-9-3-2-4-10(13)11(9)12-5-7-14-8-6-12/h9-11,13H,2-8H2,1H3/t9-,10+,11+/m1/s1 |
| InChIKey | QBYAHCABHDBVQY-VWYCJHECSA-N |
| Mol Weight | 199.29 g/mol |
| Molecular Formula | C11H21NO2 |
| Exact Mass | 199.157229 g/mol |
| Enantiomer InChIKey | QBYAHCABHDBVQY-HBNTYKKESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
TRANS-3-METHYL-TRNAS-2-(1-PYRROLIDINO)-CYClOHEXANOL
(+)-HASTANECINE
(1SR,7SR,8SR)-1-(Hydroxymethyl-7-hydroxypyrrolizidine [(1SR,7SR,8SR)-turneforcidine]
8a,N-Dimethyl-trans-decahydro-quinolinium cation
N,8-BETA-DIMETHYL-TRANS-DECAHYDROQUINOLINE
8,N-DIMETHYL-TRANS-DECAHYDROQUINOLINE;DIASTEREOMER-#1
N,8-ALPHA-DIMETHYL-TRANS-DECAHYDROQUINOLINE
1-Methoxy-2-piperidinocyclohexane
EXO-N-PYRROLIDINO-2-AMINONORBORNANE
| Title | Journal or Book | Year |
|---|---|---|
| Boranes in Synthesis. 5. The Hydroboration of Enamines with Mono- and Dialkylboranes. Asymmetric Synthesis of .beta.-Amino Alcohols of Moderate Enantiomeric Purity from Aldehyde Enamines | The Journal of Organic Chemistry | 1995 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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