4-BROMO-2,2-DIPHENYL-3-[1-(TETRAHYDRO-2H-PYRAN-2-YL-OXY)-ETHYL]-1-OXA-2-PHOSPHONIASPIRO-[4.5]-DEC-3-ENE-BROMIDE
Compound with spectra: 1 NMR
![4-BROMO-2,2-DIPHENYL-3-[1-(TETRAHYDRO-2H-PYRAN-2-YL-OXY)-ETHYL]-1-OXA-2-PHOSPHONIASPIRO-[4.5]-DEC-3-ENE-BROMIDE](/api/compound/F5XZreLgH7l.png?ph=true&h=300&w=458 "4-BROMO-2,2-DIPHENYL-3-[1-(TETRAHYDRO-2H-PYRAN-2-YL-OXY)-ETHYL]-1-OXA-2-PHOSPHONIASPIRO-[4.5]-DEC-3-ENE-BROMIDE")
| SpectraBase Compound ID | F5XZreLgH7l |
|---|---|
| InChI | InChI=1S/C27H33BrO3P.BrH/c1-21(30-24-17-9-12-20-29-24)25-26(28)27(18-10-4-11-19-27)31-32(25,22-13-5-2-6-14-22)23-15-7-3-8-16-23;/h2-3,5-8,13-16,21,24H,4,9-12,17-20H2,1H3;1H/q+1;/p-1 |
| InChIKey | SFOYFLDKPXMDEL-UHFFFAOYSA-M |
| Mol Weight | 596.3 g/mol |
| Molecular Formula | C27H33Br2O3P |
| Exact Mass | 594.053408 g/mol |
| Parent InChIKey | BGXIZDSYCQMSNP-UHFFFAOYSA-M |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
6-(1,3-Benzothiazol-2-yl)-3-(thiazol-2-yldiazenyl)pyrazolo[1,5-a]pyrimidine-2,7-diamine
2-METHOXY-4-PHENYLSELENENYL-3-[1-(TETRAHYDRO-2H-PYRAN-2-YL-OXY)-ETHYL]-1-OXA-2-PHOSPHASPIRO-[4.5]-DEC-3-ENE-2-OXIDE
5-OXO-2-(TRIFLUOROMETHYL)-5H-[1]BENZOPYRANO[2,3-b]PYRIDINE-3-CARBOXY-2',6'-XYLIDIDE
YUQOGRIZONMRAA-GMJRYDSNSA-N
2-amino-4-(3-hydroxy-4-methoxyphenyl)-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile
3-C-(4-tert-butylbenzene)-2-N,4,6-trimethyl-2-N-phenylthieno[2,3-b]pyridine-2,3-diamido
10a-hydroxy-5,7,7-trimethyl-6,6a,8,9-tetrahydrophenanthridin-10-one
(2Z)-2-[3-fluoro-2-(trifluoromethyl)-4-pyrano[3,2-b]benzofuranylidene]acetic acid ethyl ester
Methyl-3,9,20-trioxo-C-nor-9,11-seco-5.alpha.,17.alpha.-pregnan-11-oate
Diethyl (3R,4R,5S)-4-Formyl-5-(2-furyl)-3-phenylpyrrolidine-2,2-dicarboxylate
| 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 |