Atomfair 4-(Trifluoromethoxy)benzenesulfonamide C7H6F3NO3S

Description 4-(Trifluoromethoxy)benzenesulfonamide (CAS No. 1513-45-7) is a high-purity sulfonamide derivative featuring a trifluoromethoxy functional group. With the molecular formula C7H6F3NO3S , this compound is widely utilized in pharmaceutical and agrochemical research due to its unique electronic and steric properties. Its IUPAC name is 4-(trifluoromethoxy)benzenesulfonamide , and it is characterized by excellent stability and reactivity, making it a valuable intermediate in organic synthesis. This product is rigorously tested for purity and consistency, ensuring reliable performance in demanding laboratory applications. Suitable for researchers and scientists, it is available in various quantities to meet both small-scale and bulk requirements.

Description

4-(Trifluoromethoxy)benzenesulfonamide (CAS No. 1513-45-7) is a high-purity sulfonamide derivative featuring a trifluoromethoxy functional group. With the molecular formula C₇H₆F₃NO₃S, this compound is widely utilized in pharmaceutical and agrochemical research due to its unique electronic and steric properties. Its IUPAC name is 4-(trifluoromethoxy)benzenesulfonamide, and it is characterized by excellent stability and reactivity, making it a valuable intermediate in organic synthesis. This product is rigorously tested for purity and consistency, ensuring reliable performance in demanding laboratory applications. Suitable for researchers and scientists, it is available in various quantities to meet both small-scale and bulk requirements.

CAS No: 1513-45-7
Molecular Formula: C7H6F3NO3S
Molecular Weight: 241.19
Exact Mass: 241.00204871
Monoisotopic Mass: 241.00204871
IUPAC Name: 4-(trifluoromethoxy)benzenesulfonamide
SMILES: C1=CC(=CC=C1OC(F)(F)F)S(=O)(=O)N
Synonyms: 4-(Trifluoromethoxy)benzenesulfonamide, 1513-45-7, RGOJCHYYBKMRLL-UHFFFAOYSA-, DTXSID00380415, DTXCID40331441

Application

4-(Trifluoromethoxy)benzenesulfonamide is primarily employed as a key intermediate in the synthesis of bioactive molecules, including pharmaceuticals and agrochemicals. Its trifluoromethoxy group enhances lipophilicity and metabolic stability, making it valuable in drug discovery. Researchers also utilize this compound in the development of sulfonamide-based inhibitors and catalysts. Its versatility extends to material science applications, where it serves as a building block for advanced polymers and coatings.

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