Atomfair Bis(chlorosulfonyl)amine Cl2HNO4S2

Description Bis(chlorosulfonyl)amine (CAS No. 15873-42-4) is a highly reactive sulfonamide derivative with the molecular formula Cl2HNO4S2. This specialized chemical compound, also known by its IUPAC name N-chlorosulfonylsulfamoyl chloride , is widely utilized in advanced organic synthesis and industrial applications. Its unique structure features two chlorosulfonyl groups bonded to a central nitrogen atom, making it a versatile intermediate for sulfonylation and chlorination reactions. The compound is supplied as a high-purity reagent, ensuring optimal performance in demanding laboratory and production environments. Proper handling under inert conditions is recommended due to its moisture sensitivity and reactivity.

Description

Bis(chlorosulfonyl)amine (CAS No. 15873-42-4) is a highly reactive sulfonamide derivative with the molecular formula Cl₂HNO₄S₂. This specialized chemical compound, also known by its IUPAC name N-chlorosulfonylsulfamoyl chloride, is widely utilized in advanced organic synthesis and industrial applications. Its unique structure features two chlorosulfonyl groups bonded to a central nitrogen atom, making it a versatile intermediate for sulfonylation and chlorination reactions. The compound is supplied as a high-purity reagent, ensuring optimal performance in demanding laboratory and production environments. Proper handling under inert conditions is recommended due to its moisture sensitivity and reactivity.

CAS No: 15873-42-4
Molecular Formula: Cl2HNO4S2
Molecular Weight: 214.1
Exact Mass: 212.8724052
Monoisotopic Mass: 212.8724052
IUPAC Name: N-chlorosulfonylsulfamoyl chloride
SMILES: N(S(=O)(=O)Cl)S(=O)(=O)Cl
Synonyms: Bis(chlorosulfonyl)amine, 15873-42-4, Imidodisulfuryl chloride, N-chlorosulfonylsulfamoyl chloride, [(chlorosulfonyl)amino]sulfonyl chloride

Application

Bis(chlorosulfonyl)amine serves as a key precursor in the synthesis of sulfonamide-based pharmaceuticals and agrochemicals. Its reactive chlorosulfonyl groups make it valuable for creating sulfonyl chlorides and other sulfur-containing compounds. The chemical is particularly useful in polymer chemistry for modifying surface properties and creating specialty materials. Researchers also employ it as a chlorinating agent in organic transformations.

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