(E)-7-HYDROXY-2-ACETYLOXYMETHYL-ADAMANTANE
Compound with spectra: 2 NMR
| SpectraBase Compound ID | CGlHFEzL5eB |
|---|---|
| InChI | InChI=1S/C13H20O3/c1-8(14)16-7-12-10-2-9-3-11(12)6-13(15,4-9)5-10/h9-12,15H,2-7H2,1H3/t9-,10-,11-,12-,13-/m0/s1 |
| InChIKey | FRTDBHCVXWTBHC-VLJOUNFMSA-N |
| Mol Weight | 224.3 g/mol |
| Molecular Formula | C13H20O3 |
| Exact Mass | 224.141245 g/mol |
| Enantiomer InChIKey | FRTDBHCVXWTBHC-SYLRKERUSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- (Z)-5-HYDROXY-2-ACETYLOXYMETHYL-ADAMANTANE
(E)-2-METHOXY-5-TERT.-BUTYLADAMANTANE
(Z)-2-METHOXY-5-TERT.-BUTYLADAMANTANE
5-trimethylsilyladamantan-2-ol
(Z)-4-FLUOROADAMANTANE-1-CARBOXYLIC-ACID
(E)-4-FLUOROADAMANTANE-1-CARBOXYLIC-ACID
5-(trimethylstannyl)adamatan-2-ol
4-Hydroxy-1-acetyladamantane
(E)-4-CHLORO-ADAMANTANE-1-CARBOXYLIC-ACID
(E)-5-Chloro-2-trimethylsilyloxy-adamantane
(E)-4-BROMO-ADAMANTANE-1-CARBOXYLIC-ACID
| Title | Journal or Book | Year |
|---|---|---|
| Hyperconjugative Control by Remote Substituents of Diastereoselectivity in the Oxygenation of Hydrocarbons | Organic Letters | 2000 |
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.