CAS 83482-57-9: 4-(4-cumylphenoxy)phthalonitrile
Formula:C23H18N2O
InChI:InChI=1/C23H18N2O/c1-23(2,19-6-4-3-5-7-19)20-9-12-21(13-10-20)26-22-11-8-17(15-24)18(14-22)16-25/h3-14H,1-2H3
SMILES:CC(C)(c1ccccc1)c1ccc(cc1)Oc1ccc(C#N)c(c1)C#N
Synonyms:- 4-(4-alpha-Cumylphenoxy)phtalonitrile
- 4-[4-(2-Phenylpropan-2-Yl)Phenoxy]Benzene-1,2-Dicarbonitrile
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Found 6 products.
4-(4-(2-Phenylpropan-2-Yl)Phenoxy)Phthalonitrile
CAS:4-(4-(2-Phenylpropan-2-Yl)Phenoxy)PhthalonitrilePurity:99%Molecular weight:338.4g/mol4-(4-α-Cumylphenoxy)phthalonitrile
CAS:Formula:C23H18N2OPurity:>98.0%(HPLC)(N)Color and Shape:White to Almost white powder to crystalMolecular weight:338.414-(4-α-CUMYLPHENOXY)PHTHALONITRILE
CAS:Formula:C23H18N2OPurity:95%Color and Shape:SolidMolecular weight:338.40184-(4-a-Cumylphenoxy)phthalonitrile
CAS:4-(4-A-Cumylphenoxy)phthalonitrile is a phthalonitrile derivative that is used as a reagent in organic synthesis. It has been shown to be an efficient nucleophile and can be used for the substitution of electron-deficient alkenes, such as ethylbenzene and propylene. 4-(4-A-Cumylphenoxy)phthalonitrile reacts with nucleophilic compounds to form stable enolates, which are then hydrolyzed by base to produce carboxylic acids. The bathochromic shift of this compound has been observed at the λmax = 616 nm wavelength. This shift is due to the fact that the conjugated double bond does not have any pi electrons. The synthesis of 4-(4-A-Cumylphenoxy)phthalonitrile begins with the reaction of phthalonitriles with phthalocyanines or hexamPurity:Min. 95%
