99276-81-0

Basic information

• Product Name: 1,2-bis-(3,4-dicyanophenoxy)-4-tert-butylbenzene
• Synonyms: 1,2-bis-(3,4-dicyanophenoxy)-4-tert-butylbenzene
• CAS NO: 99276-81-0
• Molecular Weight: 418.455
• Mol File: 99276-81-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-bis-(3,4-dicyanophenoxy)-4-tert-butylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-bis-(3,4-dicyanophenoxy)-4-tert-butylbenzene(99276-81-0)
• EPA Substance Registry System: 1,2-bis-(3,4-dicyanophenoxy)-4-tert-butylbenzene(99276-81-0)

Safety Data

• Hazardous Substances Data: 99276-81-0(Hazardous Substances Data)

Upstream product

• 13138-53-9 4-nitrophthalic amide 
• 31643-49-9 4-Nitrophthalonitrile 
• 98-29-3 4-tert-Butylcatechol 

Relevant articles and documents

Synthesis and properties of new binuclear nickel(II) phthalocyanines

New binuclear nickel(II) phthalonitrile complexes, viz., NiII 2,2′,9(10),9′(10′),17(18),17′(18′),24(25), 24′(25′)-tetra(phenylene-1,2-dioxy)bisphthalocyanine and Ni II 2,2′,9(10),9′(10′),17(18),17′(18′), 24(25),24′(25′)-tetra(4-tert-butyl-phenylene-1,2-dioxy) bisphthalocyanine, were synthesized. The complexes were characterized by electronic spectroscopy and MALDI-TOF mass spectrometry and studied as active components for membranes of ion-selective electrodes in solutions of dicarboxylic acids.

Binuclear phthalocyanines covalently linked through two- and four-atom bridges

Binuclear phthalocyanines in which the two phthalocyanine nuclei are covalently linked through four-atom bridges, derived from catechol, have been prepared and characterized.Metal-free 2,9,16,23-tetra-(3,3-dimethylbutyl)phthalocyanine and 2,9,16,23-tetra-(2-trimethylsilylethyl)phthalocyanine were prepared as examples of non-oxygenated mononuclear phthalocyanines soluble in organic solvents.Catalytic hydrogenation of 1,2-bis-(3,4-dicyanophenyl)ethyne and 1,4-bis-(3,4-dicyanophenyl)buta-1,3-diyne gave 1,2-bis-(3,4-dicyanophenyl)ethane and 1,4-bis-(3,4-dicyanophenyl)butane respectively.From these precursors, metal-free phthalocyanine dimers containing ethylene and tetramethylene bridges, joining the phthalocyanine nuclei, were prepared.Two of the two-atom bridge phthalocyanine dimers represent the first characterized phthalocyanine dimers not containing alkoxy or oxygenated groups.