4-BROMO-2,2-DIPHENYL-3-[(TETRAHYDRO-2H-PYRAN-2-YL-OXY)-METHYL]-1-OXA-2-PHOSPHONIASPIRO-[4.5]-DEC-3-ENE-BROMIDE
Compound with spectra: 1 NMR
![4-BROMO-2,2-DIPHENYL-3-[(TETRAHYDRO-2H-PYRAN-2-YL-OXY)-METHYL]-1-OXA-2-PHOSPHONIASPIRO-[4.5]-DEC-3-ENE-BROMIDE](/api/compound/D3MdcyrxKGI.png?ph=true&h=300&w=458 "4-BROMO-2,2-DIPHENYL-3-[(TETRAHYDRO-2H-PYRAN-2-YL-OXY)-METHYL]-1-OXA-2-PHOSPHONIASPIRO-[4.5]-DEC-3-ENE-BROMIDE")
| SpectraBase Compound ID | D3MdcyrxKGI |
|---|---|
| InChI | InChI=1S/C26H31BrO3P.BrH/c27-25-23(20-29-24-16-8-11-19-28-24)31(21-12-4-1-5-13-21,22-14-6-2-7-15-22)30-26(25)17-9-3-10-18-26;/h1-2,4-7,12-15,24H,3,8-11,16-20H2;1H/q+1;/p-1 |
| InChIKey | BLHGMMYCFWFICH-UHFFFAOYSA-M |
| Mol Weight | 582.31 g/mol |
| Molecular Formula | C26H31Br2O3P |
| Exact Mass | 580.037758 g/mol |
| Parent InChIKey | VRQZXRCRLBDDTM-UHFFFAOYSA-M |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1,2,4,9-Tetramethyl-11,12-dioxatricyclo(5.3.1.1**2,6)dodecan-4,8-dien-3,10-dione
(E)-4,5-DIBROMO-3,5-DI-TERT.-BUTYL-2-PHENYL-1,2-OXAPHOSPHOL-3-ENE-2-OXIDE
6-(3,5-Dimethyl-1H-pyrazol-1-yl)-N-(2-methylphenyl)[1,2,5]oxadiazolo[3,4-b]pyrazin-5-amine
(1E)-3-CHLORO-3-METHYL-2-PHENYLSELENENYL-1-[(TETRAHYDRO-2H-PYRAN-2-YL-OXY)-METHYL]-HEPT-1-EN-1-YL-DIPHENYL-PHOSPHINE-OXIDE
6,8-DIMETHYL-1-NITROIMIDAZO-[1,2-A]-[1,8]-NAPHTHYRIDINE
1H-2-benzopyran-3-carboxamide, N-(2,5-dimethylphenyl)-4-(4-methylphenyl)-1-oxo-
1H-pyrazolo[3,4-b]pyridine, 1-(1,1-dimethylethyl)-5-[3-(4-ethyl-1-piperazinyl)-3-oxopropyl]-3,4,6-trimethyl-
(3S,4S,1'S)-(+)-3-Acetoxy-3-(1',2'-epoxyethyl-1'-methoxycarbonyl)-2-methylcyclopent-1-ene-1-carbocylic acid methyl ester
Ethyl 1,2-diamino-5-cyano-4-(4-methoxyphenyl)-6-oxo-1,6-dihydropyridine-3-carboxylate
6-Methoxy-2-phenyl-4-(phenyl)sulfonylpyrido[3,2-b]pyridine
| 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 |