Benzylthiazolium bromide is a quaternary ammonium salt characterized by its thiazole ring structure, which contributes to its unique chemical properties. It typically appears as a white to off-white crystalline solid and is soluble in polar solvents such as water and alcohols. The compound is known for its role as a reagent in organic synthesis, particularly in the formation of various thiazole derivatives and as a catalyst in certain reactions. Its quaternary ammonium nature imparts cationic characteristics, making it useful in applications involving ionic interactions. Additionally, benzylthiazolium bromide can exhibit antimicrobial properties, which may be leveraged in pharmaceutical and biocidal applications. Safety considerations should be taken into account, as with many chemical substances, including proper handling and storage to avoid exposure. Overall, benzylthiazolium bromide is a versatile compound with significant utility in both research and industrial contexts.

Benzylthiazoliumbromide

75066-50-1: 3-Benzylthiazolium bromide, 3-Benzyl-1,3-Thiazol-3-Ium Bromide

3-Benzylthiazolium Bromide is a synthetic, cyclic benzene that is used as a reagent in organic chemistry. 3-Benzylthiazolium Bromide catalyzes the formation of carbenes and aldehydes from carboxylic acid and alcohols. It also catalyzes the reverse reaction, which has been shown to occur in the presence of hydroxide ion. 3-Benzylthiazolium Bromide has been recrystallized for use in catalysis studies.

CAS 75066-50-1: Benzylthiazoliumbromide

3-Benzylthiazolium Bromide

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3-Benzylthiazol-3-Ium Bromide

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3-Benzylthiazol-3-ium bromide

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3-Benzylthiazolium Bromide

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3-Benzylthiazolium Bromide ,

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