18013-43-9

Upstream product

• 137-07-5 2-amino-benzenethiol 
• 615-22-5 2-methylmercaptobenzothiazole 
• 86134-26-1 2,5-bis-trimethylstannanyl-thiophene 
• 932-95-6 2,5-thiophenedicarboxaldehyde 
• 87230-58-8 2,5-(dibenzothiazolin-2-yl)thiophene 
• 3857-36-1 thiophene-2,5-dicarbonyl dichloride 
• 21749-63-3 2-(methylamino)benzenethiol 

Relevant academic research and scientific papers

Coplanarity driven fluorescence turn-on sensor for chromium(III) and its application for bio-imaging

New benzimidazole and benzothiazole derivatives (S1-S3) derived from thiophene-2,5-dicarboxaldehyde and 5,5′-bipyridyldicarboxaldehyde with NSN/SSS/NN binding sites were tested against various cations and anions. S3 showed selectivity toward copper(ii) io

Converting Thioether Waste into Organic Semiconductors by Carbon–Sulfur Bond Activation

A goal for human society is to convert organic waste into valuable materials. Herein, 2-(methylthio)-bezothiazole (MTBT), an important organic waste in urban runoff, was catalytically converted into a series of organic semiconductors through carbon–sulfur

Spectroscopic differences between heterocyclic benzothiazoline, -thiazole and imine containing ligands and comparison of the Co and Cu pyridine benzothiazole and imine complexes

Five heterocyclic benzothiazoline and -thiazole analogs have been synthesized and characterized by 1H NMR and IR spectroscopy. The analogs fall into two different classes, (a) those which contain one benzothiazoline group adjacent to the hetero

Synthesis, Characterization and Electron Impact Mass Spectrometry of Schiff Bases Rearranging to Oxazoline, Thiazoline and Thiazole Derivatives

A series of oxazoline compounds have been prepared by reaction of 2,6-diformyl-4-chlorophenol, 2,6-diformylpyridine or 2,5-diformylthiophen with o-aminophenol or o-aminothiophenol respectively.The oxazoline derivatives are stable both in solid state and i