75219-13-5

Usage

Structure

A derivative of benzothiazole, containing a benzene ring fused to a thiophene ring

Appearance

Yellowish crystalline powder

Usage

Commonly used in organic synthesis and as a building block in the production of pharmaceuticals and agrochemicals

Potential applications

In materials science and as a fluorescent dye

Biological activities

Antimicrobial, antioxidant, and anti-inflammatory properties, making it a target for research in drug discovery and development.

Upstream product

• 108-94-1 cyclohexanone 
• 149-30-4 2-Mercaptobenzothiazole 
• 1056477-06-5 2-bromocyclohexanone 
• 822-87-7 2-Chlorocyclohexanone 
• 120-78-5 di(benzothiazol-2-yl)disulfide 

Downstream Products

• 94862-31-4 (4-methoxy-phenyl)-carbamic acid 2-benzothiazol-2-ylsulfanyl-cyclohexyl ester 
• 75219-17-9 2-benzothiazol-2-ylsulfanyl-cyclohexanol 

Relevant academic research and scientific papers

Esterase-sensitive sulfur dioxide prodrugs inspired by modified Julia olefination

Sulfur dioxide (SO2) is an endogenously produced gaseous molecule, and is emerging as a potential gasotransmitter. Herein, we describe the first series of esterase-sensitive prodrugs inspired by modified Julia olefination as SO2 donors.

Stereoselective synthesis of electrophilic spirocyclopropanes in ionic liquids

The reaction of β-oxosulfides of benzothiazole with Michael acceptors, in liquid tetrabutylammonium bromide and sodium bicarbonate as base, allows a stereoselective synthesis of spirocyclopropanes. (C) 2000 Elsevier Science Ltd.

Conformations of 2-alkyl(aryl)thiocyclohexanones

According to the 1H NMR data, 2-alkyl(aryl)thiocyclohexanones exist mainly as axial conformers. An exception is 2-(2-benzothiazolylthio)cyclohexanone which exists mainly as equatorial conformer due to intramolecular electrostatic interactions.