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Atomfair 4-(Pentafluoro-lambda6-sulfanyl)benzaldehyde C7H5F5OS
Description 4-(Pentafluoro-lambda6-sulfanyl)benzaldehyde (CAS No. 401892-84-0) is a high-purity fluorinated aromatic aldehyde with the molecular formula C7H5F5OS . This compound features a pentafluorosulfanyl (-SF5) group, a highly electronegative and lipophilic substituent, which enhances its reactivity and stability in synthetic applications. Ideal for advanced organic synthesis, this benzaldehyde derivative is widely used in pharmaceuticals, agrochemicals, and materials science due to its unique electronic properties. Supplied as a crystalline solid with ??95% purity (GC), it is rigorously tested for consistency and quality, ensuring reliable performance in demanding research environments. Store under inert conditions to maintain stability.
Description
Description
4-(Pentafluoro-lambda6-sulfanyl)benzaldehyde (CAS No. 401892-84-0) is a high-purity fluorinated aromatic aldehyde with the molecular formula C7H5F5OS. This compound features a pentafluorosulfanyl (-SF5) group, a highly electronegative and lipophilic substituent, which enhances its reactivity and stability in synthetic applications. Ideal for advanced organic synthesis, this benzaldehyde derivative is widely used in pharmaceuticals, agrochemicals, and materials science due to its unique electronic properties. Supplied as a crystalline solid with ??95% purity (GC), it is rigorously tested for consistency and quality, ensuring reliable performance in demanding research environments. Store under inert conditions to maintain stability.
- CAS No: 401892-84-0
- Molecular Formula: C7H5F5OS
- Molecular Weight: 232.17
- Exact Mass: 231.99812676
- Monoisotopic Mass: 231.99812676
- IUPAC Name: 4-(pentafluoro-lambda6-sulfanyl)benzaldehyde
- SMILES: C1=CC(=CC=C1C=O)S(F)(F)(F)(F)F
- Synonyms: 4-(pentafluoro-lambda6-sulfanyl)benzaldehyde, 692-885-0, 401892-84-0, 4-(Pentafluorosulfanyl)benzaldehyde, 4-(Pentafluorothio)benzaldehyde
Application
4-(Pentafluoro-lambda6-sulfanyl)benzaldehyde is a versatile building block in medicinal chemistry, particularly for synthesizing SF5-containing drug candidates with improved metabolic stability. It is also employed in materials science to create fluorinated polymers and liquid crystals with enhanced thermal and chemical resistance. Researchers utilize this compound in cross-coupling reactions to introduce the pentafluorosulfanyl group into complex molecules.
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