4468-56-8

Usage

Uses

Used in Pharmaceutical Industry:
BIS-(4-N,N-DIMETHYLAMINOPHENYL) PHENYLACTONITRILE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of novel drugs with potential therapeutic applications.
Used in Materials Science:
In the field of materials science, BIS-(4-N,N-DIMETHYLAMINOPHENYL) PHENYLACTONITRILE is utilized as a component in the design and synthesis of advanced materials, leveraging its unique chemical properties to enhance material performance.
Used in Chemical Engineering:
BIS-(4-N,N-DIMETHYLAMINOPHENYL) PHENYLACTONITRILE serves as a crucial building block in chemical engineering, where it is employed in the creation of new chemical processes and products, contributing to innovation in chemical synthesis and industrial applications.
The specific role and potential uses of BIS-(4-N,N-DIMETHYLAMINOPHENYL) PHENYLACTONITRILE may vary across different industries and are dependent on the context and objectives of chemical research and development. Its versatility and unique properties position it as a promising compound for future applications in various sectors.

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 
• 151-50-8 potassium cyanide 
• 13425-25-7 malachite green oxalate 
• 773837-37-9 sodium cyanide 
• 16096-33-6 1-phenyl-1H-indole 
• 61766-63-0 2-diazo-2-phenylacetonitrile 
• 121-69-7 N,N-dimethyl-aniline 
• 87182-67-0 N,N-bis(2-methoxyethyl)-benzenamide 
• 57-12-5 cyanide^(1-) 

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 academic research and scientific papers

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.).

COMPOSITIONS AND METHODS FOR DETECTING NERVE AGENTS

The present invention provides methods and compositions for detecting, identifying and measuring the abundance of chemical nerve agents. Methods and compositions of the present invention are capable of providing selective detection of phosphorous based ne

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.

EFFECT OF STRUCTURAL FACTORS ON THE KINETICS OF THE REACTION OF THE CONJUGATE IONS OF THE TRIARYLMETHANE SERIES WITH THE CYANIDE ION

The kinetic of the raction of some triarylmethane dyes with the CN(1-) ion in aqueous solution in the range of 11.5-50 deg C were investigated by a spectrophotometric method.A correlation analysis of the results was undertaken, and on the basis of a comparison of the obtained characteristics with the corresponding parameters for the formation of triarylcarbinols it was shown that the type of control of the reactivity of the conjugate ions is independent of the nature of the nucleophilic agent.