56048-80-7

Upstream product

• 100-83-4 meta-hydroxybenzaldehyde 
• 137-07-5 2-amino-benzenethiol 

Downstream Products

• 112946-93-7 1-[2-(3-Hydroxy-phenyl)-benzothiazol-3-yl]-ethanone 
• 86135-49-1 1-{2-[3-(3-Dimethylamino-propoxy)-phenyl]-benzothiazol-3-yl}-ethanone 
• 93264-89-2 1-{2-[3-(3-Chloro-propoxy)-phenyl]-benzothiazol-3-yl}-ethanone 

Relevant academic research and scientific papers

Enantioselective organocatalytic transfer hydrogenation of α-imino esters by utilization of benzothiazoline as highly efficient reducing agent

Benzothiazoline was employed as an efficient and versatile reducing agent for the chiral phosphoric acid-catalyzed transfer hydrogenation of α-imino esters. The corresponding α-amino esters were furnished with excellent enantioselectivities. Novel and rea

Novel Calcium Antagonists. Synthesis and Structure-Activity Relationship Studies of Benzothiazoline Derivatives

A series of novel compounds having a benzothiazoline skeleton was studied for their structure-activity relationship (SAR) with respect to Ca2+ antagonist activity.As test compounds, analogues of 3-acyl-2-arylbenzothiazolines (3) were synthesize

Control of acarids using certain benzothiazoles or benzothiazolines

Compounds having either of the structures SPC1 Have strong acaricidal activity, in which R is a phenyl or naphthyl group, or phenyl with certain designated substitution. Thus, mites may be controlled on such crops as cotton by applying such compounds as 2-(1-naphthyl)benzothiazoline or 2-(5-t-butyl-2-hydroxyphenyl)benzothiazole.