4-Fluoro-1,3-benzothiazole-2-thiol is a heterocyclic compound characterized by the presence of both a benzothiazole ring and a thiol functional group. The molecular structure features a fluorine atom substituted at the 4-position of the benzothiazole, which contributes to its chemical reactivity and potential applications. This compound is typically a solid at room temperature and exhibits properties such as moderate solubility in organic solvents. The thiol group (-SH) imparts unique reactivity, allowing for potential applications in organic synthesis, medicinal chemistry, and materials science. The presence of the fluorine atom can enhance the compound's biological activity and influence its interaction with biological targets. Additionally, 4-fluoro-1,3-benzothiazole-2-thiol may exhibit specific spectral characteristics in techniques such as NMR and IR spectroscopy, aiding in its identification and characterization. Overall, this compound is of interest in various fields, including pharmaceuticals and agrochemicals, due to its unique structural features and reactivity.

4-fluoro-1,3-benzothiazole-2-thiol

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The 4-fluoro-3H-1,3-benzothiazole-2-thione is a sulfur heterocycle that can be synthesized by the reaction of 2,4-dihydroxybenzenesulfonic acid and thiourea in aqueous solution. This method yields high yields of the desired product with an efficient synthesis. The 4-fluoro-3H-1,3-benzothiazole-2-thione can be used as an intermediate for other organic compounds. The compound has been shown to be an efficient activator for lc/ms detection of small molecules.

CAS 154327-24-9: 4-fluoro-1,3-benzothiazole-2-thiol

4-fluoro-3h-1,3-benzothiazole-2-thione

Ref: 3D-FF105097

4-Fluoro-2-mercaptobenzothiazole

Ref: 54-PC902198

4-Fluorobenzo[d]thiazole-2(3H)-thione

Ref: 10-F609197

4-Fluorobenzo[d]thiazole-2(3H)-thione

Ref: IN-DA003LF2