(2-S)-4-(TRIMETHYLSILYL)-1-PHENYLBUT-3-YN-2-OL
Compound with spectra: 1 NMR
| SpectraBase Compound ID | IWcPPGTuD3P |
|---|---|
| InChI | InChI=1S/C13H18OSi/c1-15(2,3)10-9-13(14)11-12-7-5-4-6-8-12/h4-8,13-14H,11H2,1-3H3/t13-/m1/s1 |
| InChIKey | HBSGOYLLGQWALH-CYBMUJFWSA-N |
| Mol Weight | 218.37 g/mol |
| Molecular Formula | C13H18OSi |
| Exact Mass | 218.112692 g/mol |
| Enantiomer InChIKey | HBSGOYLLGQWALH-ZDUSSCGKSA-N |
| Racemate InChIKey | HBSGOYLLGQWALH-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1-Phenyl-3-(trimethylsilyl)propan-2-ol
3-PHENYL-1,1,1-TRIFLUORO-2-PROPANOL
1-Ethoxy-3-phenyl-2-propanol
3,3,3-Trideuterio-1-phenyl-2-propanol
4-Methyl-1-phenyl-3-penten-2-ol
1-Phenylhex-5-en-2-ol
3-Hydroxy-4-phenyl-2-butanone
Benzeneethanol, .alpha.-[[(1-methylethyl)amino]methyl]-
1-Phenyl-2-octanol
1-isopropoxy-3-phenyl-propan-2-ol
| Title | Journal or Book | Year |
|---|---|---|
| Practical Asymmetric Approach to Medium-Sized Carbocycles Based on the Combination of Two Ru-Catalyzed Transformations and a Lewis Acid-Induced Cyclization | Organic Letters | 2004 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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