915190-54-4

Basic information

• Product Name: 2-(3,4,5-trimethoxyphenyl)-benzo[b]thiophene-3-carbonitrile
• Synonyms: 2-(3,4,5-trimethoxyphenyl)-benzo[b]thiophene-3-carbonitrile
• CAS NO: 915190-54-4
• Molecular Weight: 325.388
• Mol File: 915190-54-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(3,4,5-trimethoxyphenyl)-benzo[b]thiophene-3-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,4,5-trimethoxyphenyl)-benzo[b]thiophene-3-carbonitrile(915190-54-4)
• EPA Substance Registry System: 2-(3,4,5-trimethoxyphenyl)-benzo[b]thiophene-3-carbonitrile(915190-54-4)

Safety Data

• Hazardous Substances Data: 915190-54-4(Hazardous Substances Data)

Upstream product

• 2856-63-5 2-Chlorophenylacetonitrile 
• 65322-86-3 Methyl 3,4,5-trimethoxydithiobenzoate 
• 24434-84-2 benzo[b]thiophene-3-carbonitrile 
• 2675-79-8 1-bromo-3,4,5-trimethoxybenzene 

Downstream Products

• 915190-58-8 C-[2-(3,4,5-trimethoxyphenyl)benzo[b]thiophen-3-yl]methylamine 

Relevant articles and documents

One-pot synthesis of 2,3-substituted benzo[b]thiophenes via Cu(i) catalysed intramolecular cyclisation from dithioesters

Efficient synthesis of benzo[b]thiophenes from o-halophenyl acetonitrile has been achieved. This novel one-pot procedure involves CuI and pivalic acid catalyzed C-S bond formation using dithioesters followed by a heterocyclization reaction. This efficient

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