6774-40-9

Basic information

• Product Name: 2-phenylbenzo[b]thiophene-3-carbonitrile
• Synonyms: 2-phenylbenzo[b]thiophene-3-carbonitrile
• CAS NO: 6774-40-9
• Molecular Weight: 235.309
• Mol File: 6774-40-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-phenylbenzo[b]thiophene-3-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenylbenzo[b]thiophene-3-carbonitrile(6774-40-9)
• EPA Substance Registry System: 2-phenylbenzo[b]thiophene-3-carbonitrile(6774-40-9)

Safety Data

• Hazardous Substances Data: 6774-40-9(Hazardous Substances Data)

Upstream product

• 312612-67-2 1-(2-(methylthio)phenyl)-2-phenylacetylene 
• 75-05-8 acetonitrile 
• 2168-78-7 methyl dithiobenzoate 
• 2856-63-5 2-Chlorophenylacetonitrile 
• 24434-84-2 benzo[b]thiophene-3-carbonitrile 
• 108-86-1 bromobenzene 
• 591-50-4 iodobenzene 

Relevant articles and documents

Copper-Catalyzed Acyloxycyanation of Alkynes with Acetonitrile: Regioselective Construction of Cyclic Acrylonitriles by 6-endo or 5-exo Cyclization

An efficient difunctionalization of alkynes by tandem iodolactonization and copper-catalyzed cyanation using acetonitrile as a cyanating reagent is reported for the first time. This approach can afford cyano-containing isocoumarin or phthalide derivatives

Synthesis of benz[c]benzothiopheno[2,3-e]azepines via Heck-type coupling and Pictet-Spengler reaction

New benz[c]benzothiopheno[2,3-e]azepine derivatives 1 of potential biological properties were synthesised in four steps from bromobenzo[b] thiophene. The synthetic pathway is based on 'Heck-type' and Pictet-Spengler reactions. Georg Thieme Verlag Stuttgar