50847-06-8

Basic information

• Product Name: 2-PHENYL-1H-IMIDAZOLE-4,5-DICARBONITRILE
• Synonyms: 2-PHENYL-1H-IMIDAZOLE-4,5-DICARBONITRILE;4,5-DICYANO-2-PHENYLIMIDAZOLE
• CAS NO: 50847-06-8
• Molecular Formula: C₁₁H₆N₄
• Molecular Weight: 194.19
• Mol File: 50847-06-8.mol
• Article Data: 5

Chemical Properties

• Melting Point: 192-196°(dec)
• Boiling Point: 540.7 °C at 760 mmHg
• Flash Point: 164.2 °C
• Appearance: /
• Density: 1.36 g/cm³
• Vapor Pressure: 9.36E-12mmHg at 25°C
• Refractive Index: 1.654
• CAS DataBase Reference: 2-PHENYL-1H-IMIDAZOLE-4,5-DICARBONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PHENYL-1H-IMIDAZOLE-4,5-DICARBONITRILE(50847-06-8)
• EPA Substance Registry System: 2-PHENYL-1H-IMIDAZOLE-4,5-DICARBONITRILE(50847-06-8)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 50847-06-8(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 95, p. 2695, 1973 DOI: 10.1021/ja00789a054

InChI:InChI=1/C11H6N4/c12-6-9-10(7-13)15-11(14-9)8-4-2-1-3-5-8/h1-5H,(H,14,15)

Upstream product

• 56029-18-6 (Z)-2-Amino-3-{[1-phenyl-meth-(E)-ylidene]-amino}-but-2-enedinitrile 
• 2004-70-8 1-methylbuta-1,3-diene 
• 51285-29-1 2-diazo-4,5-dicyano-2H-imidazole 
• 56029-18-6 2-(benzen-1-yl)methyleneamino-3-aminomaleonitrile 
• 40953-34-2 2-amino-1H-imidazole-4,5-dicarbonitrile 
• 71-43-2 benzene 

Downstream Products

• 1620141-01-6 1-butyl-3-methylimidazolium 4,5-dicyano-2-phenylimidazolate 
• 1620141-19-6 3-methyl-1-octylimidazolium 4,5-dicyano-2-phenylimidazolate 
• 888-60-8 2-phenyl-1H-imidazole-4,5-dicarboxylic acid 

Relevant articles and documents

CuOx/OMS-2 catalyzed synthesis of 4,5-dicyano-1H-imidazoles moiety: Directly access to D-A system for AIE-active mechanofluorochromic materials

Although a lot of mechanofluorochromic (MFC) materials have been reported, it still needs to be further explored due to the lack of the universal design principle. The AIE moiety molecules with D-A framework have been widely regarded as the ideal structur

Reactivity of diazoazoles and azolediazonium salts in C-azo coupling reactions

The comparative reactivity of heterocyclic diazo compounds and the corresponding diazonium salts in C-azo coupling reactions was studied using imidazole, pyrazole, and triazole derivatives as examples.The reactivities of pyrazole- and imidazole-derived di

A Convenient Synthesis of 2-Aryl-4,5-dicyanoimidazoles and -imidazolines from Diaminomaleonitrile

-