4468-56-8

Basic information

• Product Name: BIS-(4-N,N-DIMETHYLAMINOPHENYL) PHENYLACTONITRILE
• Synonyms: MALACHITE GREEN LEUCONITRILE;BIS-(4-N,N-DIMETHYLAMINOPHENYL) PHENYLACTONITRILE
• CAS NO: 4468-56-8
• Molecular Formula: C₂₄H₂₅N₃
• Molecular Weight: 355.48
• Mol File: 4468-56-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 506.8°Cat760mmHg
• Flash Point: 212.5°C
• Appearance: /
• Density: 1.115g/cm³
• Vapor Pressure: 2.15E-10mmHg at 25°C
• Refractive Index: 1.625
• CAS DataBase Reference: BIS-(4-N,N-DIMETHYLAMINOPHENYL) PHENYLACTONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: BIS-(4-N,N-DIMETHYLAMINOPHENYL) PHENYLACTONITRILE(4468-56-8)
• EPA Substance Registry System: BIS-(4-N,N-DIMETHYLAMINOPHENYL) PHENYLACTONITRILE(4468-56-8)

Safety Data

• Hazardous Substances Data: 4468-56-8(Hazardous Substances Data)

Usage

General Description

BIS-(4-N,N-DIMETHYLAMINOPHENYL) PHENYLACTONITRILE is a chemical compound with the formula C28H24N2. It is commonly used as a building block in organic synthesis, particularly in the development of new functional materials and pharmaceuticals. BIS-(4-N,N-DIMETHYLAMINOPHENYL) PHENYLACTONITRILE is characterized by its aromatic ring structure, as well as the presence of amino and nitrile functional groups, which confer unique reactivity and properties. BIS-(4-N,N-DIMETHYLAMINOPHENYL) PHENYLACTONITRILE has potential applications in various industries, including medicine, materials science, and chemical engineering. Its precise role and potential uses may vary depending on the specific context and the goals of chemical research and development.

InChI:InChI=1/C24H25N3/c1-26(2)22-14-10-20(11-15-22)24(18-25,19-8-6-5-7-9-19)21-12-16-23(17-13-21)27(3)4/h5-17H,1-4H3

Upstream product

• 10309-95-2 malachit green 
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• 57-12-5 cyanide^(1-) 
• 773837-37-9 sodium cyanide 
• 13425-25-7 malachite green oxalate 
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Downstream Products

• 510-13-4 1,1-bis(4-dimethylaminophenyl)-1-phenyl-methanol 
• 33560-61-1 bis-(p-N,N-dimethylaminophenyl)phenylmethyl ethyl ether 
• 97877-99-1 radical of leucobase of Malachite Green 
• 10309-95-2 malachit green 
• 1206192-86-0 1,1-bis(4-dimethylaminophenyl)-1-phenyl-2-propanone oxime 
• 1206192-87-1 α,α-bis(4-dimethylaminophenyl)phenylacetic acid 

Relevant articles and documents

Gold-Catalyzed Oxidative Cross-Coupling Reactions among Two Distinct Arenes and One Gold Carbene with Phosphoric Acids as Cocatalysts

Gold-catalyzed oxidative cross-coupling reactions of two distinct arenes with one gold carbene furnish triarylmethane products. Notably, competitive homo-coupling reactions are efficiently suppressed with a phosphoric acid as co-catalyst (10 mol%) in THF. These cross-coupling reactions have a wide scope of applicable substrates, with respect to indoles, arylamines, and α-aryl diazo cyanides or esters. Our mechanistic analysis indicates that the basicity of the arylanilines greatly affects the cross-coupling efficiency. (Figure presented.).

Photochemistry and photophysics of triarylmethane dye leuconitriles

The photochemical reactions of crystal violet leuconitrile (CVCN) were investigated by the means of product analysis and trapping experiments, laser flash and steady-state photolysis, and steady-state fluorescence. The influence of oxygen on the reaction was examined in detail. The photochemistry of malachite green leuconitrile (MGCN), basic fuchsin leuconitrile (BFCN), and crystal violet leucomethyl (CVMe) and leucobenzyl (CVBn), as well as triphenylacetonitrile, was studied. The results suggest ionization occurs from S1, while the di-π-methane reaction is the photochemical route from T1.