| Identification | Back Directory | [Name]
1,3-Bis(2,6-diisopropylphenyl)-2,2-difluoro-2,3-dihydro-1H-imidazole | [CAS]
1314657-40-3 | [Synonyms]
PhenoFluor
PhenoFluorTM
PhenofluorTM solution
1,3-bis(2,6-diisopropylphenyl)-2,2-difluoroimidazole
1,3-Bis(2,6-di-i-propylphenyl)-2,2-difluoroiMidazoline (PhenoFluor
1,3-Bis(2,6-diisopropylphenyl)-2,2-difluoro-2,3-dihydro-1H-imidazole
2,2-difluoro-2,3-dihydro-1,3-bis(2,6-diisopropylphenyl)-1H-iMidazole
N,N'-1,3-Bis(2,6-diisopropylphenyl)-2,2-difluoro-2,3-dihydro-1H-imidazole
N,N'-1,3-Bis(2,6-diisopropylphenyl)-2,2-difluoro-2,3-dihydro-1H-imidazole
1,3-Bis[2,6-bis(1-methylethyl)phenyl]-2,2-difluoro-2,3-dihydro-1H-imidazole
1H-Imidazole, 1,3-bis[2,6-bis(1-methylethyl)phenyl]-2,2-difluoro-2,3-dihydro-
1,3-Bis(2,6-di-i-propylphenyl)-2,2-difluoroiMidazoline, Min. 85% (PhenoFluor | [Molecular Formula]
C27H36F2N2 | [MDL Number]
MFCD22377831 | [MOL File]
1314657-40-3.mol | [Molecular Weight]
426.58 |
| Hazard Information | Back Directory | [Uses]
1,3-Bis(2,6-diisopropylphenyl)-2,2-difluoro-2,3-dihydro-1H-imidazole is used in the deoxyfluorination of heteroaromatic phenols. It also functions as a reagent used in the functional group tolerant synthesis of alkyl aryl ethers from phenols and alcohols. | [Uses]
PhenoFluor™ reagent is utilized in deoxyfluorination of phenols, without activation of the substrate, to provide ipso substitution to the corresponding aryl fluoride.1 |
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