17983-41-4

Upstream product

• 107-14-2 chloroacetonitrile 
• 17865-11-1 (4-(trimethylsilyl)phenyl)boronic acid 
• 6999-03-7 1-bromo-4-(trimethylsilyl)benzene 
• 1071-36-9 sodium cyanoacetate 

Downstream Products

• 23858-75-5 ethyl 2-cyano-2-(4-(trimethylsilyl)phenyl)acetate 
• 5112-74-3 2-(4-trimethylsilanyl-phenyl)-propionitrile 

Relevant academic research and scientific papers

Acrylonitrile compound as well as preparation method and application thereof

The invention relates to the field of insecticides and acaricides, and discloses an acrylonitrile compound as well as a preparation method and application thereof, and the trimethylsilyl phenyl acrylonitrile compound has a structure as shown in a formula (I). The acrylonitrile compound with a novel structure provided by the invention can be applied to prevention and control of agricultural pest mites.

Design, synthesis and acaricidal activities of Cyflumetofen analogues based on carbon-silicon isosteric replacement

The application of a carbon-silicon bioisosteric replacement strategy to find new acaricides with improved properties led to the discovery of Sila-Cyflumetofen 6B, a novel and highly potent acaricide. The essential t-butyl group in the beta-ketonitrile ac

Silicon acyl acetonitrile compound as well as preparation method and application thereof (by machine translation)

In particular, the present invention relates to a compound containing a, silicon acyl acetonitrile compound, or a stereoisomer thereof, or a. stereoisomer thereof, or a salt thereof, wherein the compound of the, present invention I I has excellent, acaric

Synthesis of α-Aryl nitriles through palladium-catalyzed decarboxylative coupling of cyanoacetate salts with aryl halides and triflates

Worth its salt: The palladium-catalyzed decarboxylative coupling of the cyanoacetate salt as well as its mono- and disubstituted derivatives with aryl chlorides, bromides, and triflates is described (see scheme). This reaction is potentially useful for the preparation of a diverse array of α-aryl nitriles and has good functional group tolerance. S-Phos=2-(2,6- dimethoxybiphenyl)dicyclohexylphosphine), Xant-Phos=4,5-bis(diphenylphosphino)- 9,9-dimethylxanthene. Copyright