4-Chloro-1,3-benzothiazole is an organic compound characterized by its heterocyclic structure, which includes both a benzene ring and a thiazole ring. The presence of a chlorine atom at the 4-position of the benzothiazole contributes to its reactivity and potential applications in various chemical processes. This compound typically appears as a solid and is known for its relatively low solubility in water, while being more soluble in organic solvents. It exhibits properties such as moderate stability under standard conditions, but it can undergo reactions typical of both aromatic and heterocyclic compounds, including electrophilic substitution and nucleophilic attack. 4-Chloro-1,3-benzothiazole is often utilized in the synthesis of pharmaceuticals, agrochemicals, and dyes, owing to its ability to act as a building block in organic synthesis. Additionally, it may possess biological activity, making it of interest in medicinal chemistry. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested.

4-Chloro-1,3-benzothiazole

3048-45-1: 4-Chloro-benzothiazole, 4-Chlorobenzothiazole, Benzothiazole, 4-chloro-, T56 Bn Dsj Ig

Benzothiazole, 4-chloro-

4-Chlorobenzo[d]thiazole is a furan-containing molecule that has been shown to have antitrypanosomal activity in vitro. The nitro group on the molecule may be responsible for its trypanocidal activity, since it can form reactive oxygen species. 4-Chlorobenzo[d]thiazole also has the ability to kill epimastigotes in vitro and exhibits death of cells in culture with low doses. This molecule is effective against trypanosomes and may be used as an antitrypanosomal agent.

CAS 3048-45-1: 4-Chloro-1,3-benzothiazole

Benzothiazole, 4-chloro-

Ref: IN-DA00309R

4-Chlorobenzo[d]thiazole

Ref: 3D-FC144199

4-chloro-1,3-benzothiazole

Ref: 54-OR480399

4-Chlorobenzothiazole

Ref: 10-F076309