4-BROMO-5-BUTYL-5-METHYL-2,2-DIPHENYL-3-[(TETRAHYDRO-2H-PYRAN-2-YL-OXY)-METHYL]-2,5-DIHYDRO-1,2-OXAPHOSPHOL-2-IUM-BROMIDE
Compound with spectra: 1 NMR
![4-BROMO-5-BUTYL-5-METHYL-2,2-DIPHENYL-3-[(TETRAHYDRO-2H-PYRAN-2-YL-OXY)-METHYL]-2,5-DIHYDRO-1,2-OXAPHOSPHOL-2-IUM-BROMIDE](/api/compound/FLoug4bzAn.png?ph=true&h=300&w=458 "4-BROMO-5-BUTYL-5-METHYL-2,2-DIPHENYL-3-[(TETRAHYDRO-2H-PYRAN-2-YL-OXY)-METHYL]-2,5-DIHYDRO-1,2-OXAPHOSPHOL-2-IUM-BROMIDE")
| SpectraBase Compound ID | FLoug4bzAn |
|---|---|
| InChI | InChI=1S/C26H33BrO3P.BrH/c1-3-4-18-26(2)25(27)23(20-29-24-17-11-12-19-28-24)31(30-26,21-13-7-5-8-14-21)22-15-9-6-10-16-22;/h5-10,13-16,24H,3-4,11-12,17-20H2,1-2H3;1H/q+1;/p-1 |
| InChIKey | CLHBHBOEXHYBMW-UHFFFAOYSA-M |
| Mol Weight | 584.3 g/mol |
| Molecular Formula | C26H33Br2O3P |
| Exact Mass | 582.053408 g/mol |
| Parent InChIKey | XWVSBMDZTTVJRJ-UHFFFAOYSA-M |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
2,2-Diacetyl-5-keto-4-triphenylphosphoranylidene-tetrahydrofuran-3-carboxylic acid methyl ester
2-methyl-N-phenylindole-3-sulfonic acid phenyl ester
5,7-Dimethyl-8-oxo-2,5-epoxybicyclo[5.3.0]decan-1-ol
6-Methylindolo[1,2-c]quinazoline
8-METHOXY-2,3-DIHYDRO-1-CYClOPENT-[A]-ACRIDIN-11(6H)-ONE
2-(2,4-dimethylphenyl)-N-[2-(trifluoromethyl)phenyl]-4-quinolinecarboxamide
(2E)-2-(3,4-diethoxy-5-iodobenzylidene)[1,3]thiazolo[3,2-a]benzimidazol-3(2H)-one
N-[(1R,2S,3R,4S)-3-(4-Methoxybenzoylamino)-4,7,7-trimethylbicyclo[2.2.1]hept-2-yl]pyrazine-2-carboxamide
2-ISOBUTYRYLAMINO-6-(BETA-D-RIBOFURANOSYL)-7H-PYRROLO-[2,3-D]-PYRIMIDIN-4(3H)-ONE
1H-pyrazolo[3,4-b]pyridine, 1-(1,1-dimethylethyl)-5-[3-[4-(4-methoxyphenyl)-1-piperazinyl]-3-oxopropyl]-3,4,6-trimethyl-
| Title | Journal or Book | Year |
|---|---|---|
| Bifunctionalized Allenes. Part XV. Synthesis of 2,5-dihydro-1,2-oxaphospholes by Electrophilic Cyclization Reaction of Phosphorylated α-Hydroxyallenes | Molecules | 2014 |