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73340-33-7

Phenol, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis[2-nitro-

Catalog#: AR01HAUE  |   CAS#: 73340-33-7  |   MDL#:  |   MF: C15H8F6N2O6  |   MW: 426.2242

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Catalog Number AR01HAUE
Chemical Name Phenol, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis[2-nitro-
CAS Number 73340-33-7
Molecular Formula C15H8F6N2O6
Molecular Weight 426.2242
SMILES [O-][N+](=O)c1cc(ccc1O)C(C(F)(F)F)(C(F)(F)F)c1ccc(c(c1)[N+](=O)[O-])O

$Name$ is a versatile compound commonly used in chemical synthesis for its ability to act as a potent electrophile. In particular, Phenol, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis[2-nitro- has found significant application as a reagent in various organic reactions due to its electron-withdrawing properties and unique structural features.One key application of Phenol, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis[2-nitro- in chemical synthesis is its role as a substrate in nucleophilic aromatic substitution reactions. The presence of nitro groups and trifluoromethyl moieties in the compound makes it an attractive candidate for reactions involving nucleophilic attack, allowing for the introduction of functional groups at specific positions on the aromatic ring.Additionally, Phenol, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis[2-nitro- can serve as a precursor in the synthesis of various organic compounds with desired properties. Its unique structure offers opportunities for further functionalization through derivatization, enabling the creation of novel molecules for a wide range of applications in organic chemistry.Overall, the strategic placement of electron-withdrawing groups in Phenol, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis[2-nitro- makes it a valuable tool in chemical synthesis, allowing for precise control over reactivity and selectivity in various organic transformations.
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