5-[(Benzoylamino)methyl]thiophene-2-sulfonyl chloride is a chemical compound characterized by its sulfonyl chloride functional group, which is known for its reactivity and utility in organic synthesis. This compound features a thiophene ring, a five-membered aromatic heterocycle containing sulfur, which contributes to its unique electronic properties. The presence of the benzoylamino group indicates that it has an amide linkage, enhancing its potential for further chemical modifications. As a sulfonyl chloride, it is likely to be a potent electrophile, making it useful in acylation reactions and the synthesis of sulfonamides. The compound is typically handled with care due to its reactivity, particularly with water and alcohols, which can lead to the release of hydrochloric acid. Its applications may extend to pharmaceuticals, agrochemicals, and materials science, where it can serve as an intermediate in the synthesis of more complex molecules. Proper safety measures should be observed when working with this compound due to its corrosive nature and potential health hazards.

5-[(benzoylamino)methyl]thiophene-2-sulfonyl chloride

138872-44-3: 5-{[(Phenylcarbonyl)Amino]Methyl}Thiophene-2-Sulfonyl Chloride, 5-[(benzoylamino)methyl]-2-Thiophenesulfonylchloride

2-Thiophenesulfonyl chloride, 5-[(benzoylamino)methyl]-

5-[(Benzoylamino)methyl]thiophene-2-sulphonyl chloride

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CAS 138872-44-3: 5-[(benzoylamino)methyl]thiophene-2-sulfonyl chloride

2-Thiophenesulfonyl chloride, 5-[(benzoylamino)methyl]-

Ref: IN-DA0019QK

5-[(Benzoylamino)methyl]thiophene-2-sulphonyl chloride

Ref: 54-OR25366

5-[(Benzoylamino)methyl]thiophene-2-sulphonyl chloride

Ref: 3D-NFA87244