55368-38-2

Basic information

• Product Name: Benzonitrile, 4,4'-(2,5-thiophenediyl)bis-
• CAS NO: 55368-38-2
• Molecular Formula: C18H10N2S
• Molecular Weight: 286.357
• Mol File: 55368-38-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzonitrile, 4,4'-(2,5-thiophenediyl)bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzonitrile, 4,4'-(2,5-thiophenediyl)bis-(55368-38-2)
• EPA Substance Registry System: Benzonitrile, 4,4'-(2,5-thiophenediyl)bis-(55368-38-2)

Safety Data

• Hazardous Substances Data: 55368-38-2(Hazardous Substances Data)

Upstream product

• 3141-27-3 2,5-dibromothiophen 
• 171364-82-2 4-cyanophenylboronic acid pinacol ester 
• 126747-14-6 4-cyanophenylboronic acid 
• 188290-36-0 thiophene 
• 623-00-7 4-bromobenzenecarbonitrile 
• 18245-28-8 2-(trimethylsilyl)thiophene 
• 145483-63-2 2,5-bis(tributylstannyl)thiophene 

Downstream Products

• 193903-62-7 4,4′-(thiophene-2,5-diyl)dibenzaldehyde 
• 80498-80-2 1,4,5,6,1',4',5',6'-octahydro-2,2'-(4,4'-thiophene-2,5-diyl-diphenyl)-bis-pyrimidine 
• 80498-78-8 4,5,4',5'-tetrahydro-1H,1'H-2,2'-(4,4'-thiophene-2,5-diyl-diphenyl)-bis-imidazole 

Relevant articles and documents

Metal-Free Photocatalytic Hydrogenation Using Covalent Triazine Polymers

Photocatalytic hydrogenation of biomass-derived organic molecules transforms solar energy into high-energy-density chemical bonds. Reported herein is the preparation of a thiophene-containing covalent triazine polymer as a photocatalyst, with unique donor-acceptor units, for the metal-free photocatalytic hydrogenation of unsaturated organic molecules. Under visible-light illumination, the polymeric photocatalyst enables the transformation of maleic acid into succinic acid with a production rate of about 2 mmol g?1 h?1, and furfural into furfuryl alcohol with a production rate of about 0.5 mmol g?1 h?1. Great catalyst stability and recyclability are also measured. Given the structural diversity of polymeric photocatalysts and their readily tunable optical and electronic properties, metal-free photocatalytic hydrogenation represents a highly promising approach for solar energy conversion.

Synthesis and evaluation of thiophene-based guanylhydrazones (iminoguanidines) efficient against panel of voriconazole-resistant fungal isolates

A series of new thiophene-based guanylhydrazones (iminoguanidines) were synthesized in high yields using a straightforward two-step procedure. The antifungal activity of compounds was evaluated against a wide range of medicaly important fungal strains inc

Direct 2-arylation of thiophene using low loading of a phosphine-free palladium catalyst

The direct coupling of aryl halides with thiophene would be a considerable advantage for sustainable development because of only HBr associated with a base as by-product is formed and the number of steps to prepare these compounds is less than in more cla