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Usage

Uses

Used in Fluorescent Labeling:
2-(4'-diethylaminophenyl)benzothiazole is used as a fluorescent dye for fluorescent labeling, enabling the visualization and tracking of molecules in biological systems due to its strong fluorescence.
Used in Organic Light-Emitting Diodes (OLEDs):
In the field of optoelectronics, 2-(4'-diethylaminophenyl)benzothiazole is utilized as a key component in the development of OLEDs, where its fluorescence contributes to the efficient emission of light in these devices.
Used in Fluorescent Sensors:
2-(4'-diethylaminophenyl)benzothiazole is employed as a sensing element in fluorescent sensors, leveraging its fluorescence properties to detect and measure the presence of specific analytes in various environments.
Used in the Development of New Materials and Technologies:
2-(4'-diethylaminophenyl)benzothiazole is also used as a component in the research and development of innovative materials and technologies, particularly within the optoelectronics sector, to enhance performance and explore new applications.

Upstream product

• 120-21-8 4-Diethylaminobenzaldehyde 
• 137-07-5 2-amino-benzenethiol 

Relevant academic research and scientific papers

Fast and high-efficiency synthesis of 2-substituted benzothiazoles via combining enzyme catalysis and photoredox catalysis in one-pot

An efficient and green method, combining enzymatic and visible-light catalysis for synthesis of the widely applicable 2-substituted benzothiazoles, has been developed. This method features a relay catalysis protocol consisting of biocatalytic promiscuity

One-pot synthesis of benzimidazoles and benzothiazoles in the presence of Fe(HSO4)3 as a new and efficient oxidant

A series of substituted benzimidazoles and benzothiazoles were prepared through the one-pot reaction of ophenylenediamine and o-aminothiophenol with various aldehydes in the presence of ferric hydrogensulfate both in EtOH and water as solvent. The reactions proceed smoothly in excellent yield, high chemoselectivity and with an easy work-up.

Novel green procedure for the synthesis of 2-arylbenzothiazoles under microwave irradiation in Peg 200 or Peg 400

An improved green procedure for the synthesis of 2-aryl- and 2-hetarylbenzothiazoles by condensation of equivalent amounts of 2,2'-diaminodiphenyldisulfides or 2-aminothiophenols and various aromatic aldehydes in PEG 200/400 under microwave irradiation has been developed. This method allows the synthesis of 2-arylbenzothiazoles in high yields and with high purity regardless of the state of the starting compounds (liquid or solid) or the nature of the substituents in the aromatic ring. Copyright Taylor & Francis Group, LLC.

Benzazole compounds

There are disclosed herein benzazole compounds, exemplified by 2-(4-aminophenyl)benzothiazole and analogues or salts thereof, which exhibit very significant selective cytotoxic activity in respect of tumor cells, especially breast cancer cells, and which provide potentially useful chemotherapeutic agents for treatment of breast cancer.