Description
4-Fluoro-N,N-dimethylbenzenesulfonamide (CAS No. 383-31-3) is a high-purity sulfonamide derivative with the molecular formula C8H10FNO2S. This compound features a fluorine-substituted benzene ring and a dimethylsulfonamide functional group, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 203.23 g/mol, it is characterized by its excellent stability and reactivity under controlled conditions. Ideal for researchers and scientists, this product is rigorously tested for purity and consistency, ensuring reliable performance in advanced chemical applications. Available in various quantities to suit laboratory and industrial needs.
Properties
- CAS Number: 383-31-3
- Complexity: 250
- IUPAC Name: 4-fluoro-N,N-dimethyl-benzenesulfonamide
- InChI: InChI=1S/C8H10FNO2S/c1-10(2)13(11,12)8-5-3-7(9)4-6-8/h3-6H,1-2H3
- InChI Key: WURMPFYVFDHATI-UHFFFAOYSA-N
- Exact Mass: 203.04162790
- Molecular Formula: C8H10FNO2S
- Molecular Weight: 203.24
- SMILES: CN(C)S(=O)(=O)C1=CC=C(C=C1)F
- Topological: 45.8
- Monoisotopic Mass: 203.04162790
- Synonyms: 4-fluoro-N,N-dimethylbenzenesulfonamide, 383-31-3, N,N-Dimethyl 4-fluorobenzenesulfonamide, MFCD01211990, SCHEMBL642787, DTXSID20355403, WURMPFYVFDHATI-UHFFFAOYSA-N, STK078373, AKOS003265996, N,N-dimethyl4-fluorobenzenesulfonamide, SB77509, [(4-fluorophenyl)sulfonyl]dimethylamine, 4-Fluoro-N,N-dimethyl-benzenesulfonamide, DS-17680, SY096663, 4-fluoro-N,N-dimethyl-benzene sulfonamide, DB-361227, CS-0042877, ST50692674, 4-fluoro-1-(N,N-dimethylaminosulfonyl)benzene, N11559, Z45527550, 4-FLUORO-N~1~,N~1~-DIMETHYL-1-BENZENESULFONAMIDE
Application
4-Fluoro-N,N-dimethylbenzenesulfonamide is widely used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive sulfonamide group makes it valuable for designing sulfa-drug analogs and other bioactive molecules. Researchers also employ it in material science for developing specialty polymers and coatings. Additionally, it serves as a building block in medicinal chemistry for fluorine-containing compound libraries.
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