2,1,3-Benzothiadiazole-5-carbonyl chloride is a chemical compound characterized by its unique structure, which includes a benzothiadiazole moiety—a bicyclic structure containing both sulfur and nitrogen atoms. This compound features a carbonyl chloride functional group, making it a reactive acyl chloride. It is typically used in organic synthesis, particularly in the preparation of various derivatives and as an intermediate in the production of pharmaceuticals and agrochemicals. The presence of the carbonyl chloride group indicates that it can undergo nucleophilic substitution reactions, making it valuable for introducing acyl groups into other molecules. Additionally, the benzothiadiazole framework is known for its applications in materials science, particularly in the development of organic semiconductors and dyes. The compound is likely to be a solid at room temperature and may exhibit moderate to high stability under standard conditions, although it should be handled with care due to the reactivity of the acyl chloride functional group. Proper safety precautions should be taken when working with this compound, as it may release hydrochloric acid upon hydrolysis.

2,1,3-benzothiadiazole-5-carbonyl chloride

321309-31-3: 2,1,3-Benzothiadiazole-5-carbonyl chloride is a chemical compound characterized by its unique structure, which includes a benzothiadiazole moiety—a bicyclic structure containing both sulfur and nitrogen atoms. This compound features a carbonyl chloride functional group, making it a reactive acyl chloride. It is typically used in organic synthesis, particularly in the preparation of various derivatives and as an intermediate in the production of pharmaceuticals and agrochemicals. The presence of the carbonyl chloride group indicates that it can undergo nucleophilic substitution reactions, making it valuable for introducing acyl groups into other molecules. Additionally, the benzothiadiazole framework is known for its applications in materials science, particularly in the development of organic semiconductors and dyes. The compound is likely to be a solid at room temperature and may exhibit moderate to high stability under standard conditions, although it should be handled with care due to the reactivity of the acyl chloride functional group. Proper safety precautions should be taken when working with this compound, as it may release hydrochloric acid upon hydrolysis.

CAS 321309-31-3

2,1,3-benzothiadiazole-5-carbonyl chloride

2,1,3-Benzothiadiazole-5-carbonyl chloride

Ref: IN-DA00C87R

2,1,3-Benzothiadiazole-5-carbonyl chloride

Ref: 54-OR23125