28442-37-7

Basic information

• Product Name: 1,1'-Biphenyl, 4,4'-dimethyl-3,3'-dinitro-
• Synonyms: 1,1'-Biphenyl,4,4'-dimethyl-3,3'-dinitro;4,4'-dimethyl-3,3'-dinitro-1,1'-biphenyl;4,4'-Dimethyl-3,3'-dinitrobiphenyl
• CAS NO: 28442-37-7
• Molecular Formula: C14H12N2O4
• Molecular Weight: 272.26
• Mol File: 28442-37-7.mol
• Article Data: 1

Chemical Properties

• Melting Point: 175-176 °C(Solv: benzene (71-43-2))
• Boiling Point: 419.7±45.0 °C(Predicted)
• Density: 1.290±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,1'-Biphenyl, 4,4'-dimethyl-3,3'-dinitro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1'-Biphenyl, 4,4'-dimethyl-3,3'-dinitro-(28442-37-7)
• EPA Substance Registry System: 1,1'-Biphenyl, 4,4'-dimethyl-3,3'-dinitro-(28442-37-7)

Safety Data

• Hazardous Substances Data: 28442-37-7(Hazardous Substances Data)

Upstream product

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Relevant articles and documents

Carbon-carbon bond forming reactions in supercritical carbon dioxide in the presence of a supported palladium catalyst

The reaction of aryl iodides or vinyl triflates with a variety of olefins in supercritical carbon dioxide (scCO2), in the presence of triethylamine and palladium on carbon, has been investigated. Methyl acrylate, styrene and acrylonitrile afford vinylic substitution products. Butenone reacts with aryl iodides to form a mixture of vinylic substitution and hydroarylation (formal conjugate addition) products. n-Butyl, vinyl ether gives rise to the formation of products arising from the α- and β- arylation process.