876500-72-0

Basic information

• Product Name: 6-TRIFLUOROMETHOXYBENZOTHIAZOLE
• Synonyms: 6-TRIFLUOROMETHOXYBENZOTHIAZOLE;6-(Trifluoromethoxy)benzo[d]thiazole
• CAS NO: 876500-72-0
• Molecular Formula: C₈H₄F₃NOS
• Molecular Weight: 219.18
• Mol File: 876500-72-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 228.8±35.0 °C(Predicted)
• Appearance: /
• Density: 1.494±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: -0.13±0.10(Predicted)
• CAS DataBase Reference: 6-TRIFLUOROMETHOXYBENZOTHIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-TRIFLUOROMETHOXYBENZOTHIAZOLE(876500-72-0)
• EPA Substance Registry System: 6-TRIFLUOROMETHOXYBENZOTHIAZOLE(876500-72-0)

Safety Data

• Hazardous Substances Data: 876500-72-0(Hazardous Substances Data)

Usage

General Description

6-Trifluoromethoxybenzothiazole is a chemical compound with the molecular formula C8H5F3NOS. It is a heterocyclic aromatic compound that contains a benzothiazole ring with a trifluoromethoxy group attached to it. 6-TRIFLUOROMETHOXYBENZOTHIAZOLE has been studied for its potential applications in materials science, specifically as a building block in the synthesis of organic electronic materials. It has also been studied for its potential use as a fluorescent probe in various biochemical and medical research applications. Additionally, 6-trifluoromethoxybenzothiazole may have potential utility in the development of pharmaceuticals due to its intriguing chemical structure and potential biological activity.

Upstream product

• 124-38-9 carbon dioxide 
• 1744-22-5 Riluzole 

Downstream Products

• 1744-22-5 Riluzole 

Relevant articles and documents

Photoelectrochemical cross-dehydrogenative coupling of benzothiazoles with strong aliphatic C-H bonds

A photoelectrochemical strategy for the cross-dehydrogenative coupling of unactivated aliphatic hydrogen donors (e.g.alkanes) with benzothiazoles is reported. We used tetrabutylammonium decatungstate as the photocatalyst to activate strong C(sp3)-H bonds in the chosen substrates, while electrochemistry scavenged the extra electrons.

Synthesis of benzothiazoles from 2-aminobenzenethiols in the presence of a reusable polythiazolium precatalyst under atmospheric pressure of carbon dioxide

Synthesis of benzothiazoles from 2-aminobenzenethiols and carbon dioxide was carried out using poly(3,4-dimethyl-5-vinylthiazolium) iodide as a precatalyst to in situ generation of NHCs by deprotonation. The reaction was successfully carried out under mild conditions (1 atm of CO2 and 60–70 °C) with a broad substrate scope and functional group tolerance. The precatalyst salt was recovered and reused for several times without any loss of activity.