Benzothiazole, 2-iodo- is an organic compound characterized by the presence of both a benzothiazole ring and an iodine substituent at the second position. This compound features a bicyclic structure that consists of a benzene ring fused to a thiazole ring, which contains a sulfur and a nitrogen atom. The introduction of the iodine atom enhances its reactivity, making it useful in various chemical reactions, including electrophilic substitutions and coupling reactions. Benzothiazole derivatives are known for their applications in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. The compound typically exhibits moderate solubility in organic solvents and may have varying degrees of stability depending on environmental conditions. Additionally, it may display biological activity, which can be of interest in medicinal chemistry. Safety data should be consulted for handling and exposure guidelines, as halogenated compounds can pose health risks. Overall, 2-iodobenzothiazole serves as a valuable building block in synthetic organic chemistry.

Benzothiazole, 2-iodo-

2-Iodobenzothiazole

2-iodo-1,3-benzothiazole

2-Iodobenzothiazole is a synthetic chemical that is used in organic synthesis as a cross-coupling agent. It has been shown to react with primary amines and nucleophilic attack by halides, forming halonium ions. 2-Iodobenzothiazole is also an effective coupling partner for perfluorinated aryl boronic acids and quaternization of tertiary amines. The compound has been shown to react with vitamin B1, forming covalent bonds. 2-Iodobenzothiazole can be used as a palladium complex catalyst in the synthesis of amines or vinylene compounds.

CAS 1123-99-5: Benzothiazole, 2-iodo-

2-Iodobenzothiazole

Ref: 10-F076087

2-Iodobenzothiazole

Ref: 3B-I0938

2-iodo-1,3-benzothiazole

Ref: 54-OR480499

2-Iodobenzothiazole

Ref: 3D-FI153588

2-Iodobenzo[d]thiazole

Ref: IN-DA0082NZ