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Atomfair Phenyl 4-fluorobenzenesulfonate C12H9FO3S
Description Phenyl 4-fluorobenzenesulfonate (CAS No. 13656-61-6) is a high-purity sulfonate ester with the molecular formula C12H9FO3S . This compound is characterized by its phenyl and 4-fluorophenyl groups linked via a sulfonate bridge, making it a valuable intermediate in organic synthesis and pharmaceutical research. It is supplied as a crystalline solid with exceptional purity (>98%) to ensure consistency in experimental results. Ideal for use in nucleophilic substitution reactions, cross-coupling methodologies, and as a precursor for advanced material synthesis. Suitable for researchers in medicinal chemistry, materials science, and chemical engineering. Store in a cool, dry place away from light and moisture to…
Description
Description
Phenyl 4-fluorobenzenesulfonate (CAS No. 13656-61-6) is a high-purity sulfonate ester with the molecular formula C12H9FO3S. This compound is characterized by its phenyl and 4-fluorophenyl groups linked via a sulfonate bridge, making it a valuable intermediate in organic synthesis and pharmaceutical research. It is supplied as a crystalline solid with exceptional purity (>98%) to ensure consistency in experimental results. Ideal for use in nucleophilic substitution reactions, cross-coupling methodologies, and as a precursor for advanced material synthesis. Suitable for researchers in medicinal chemistry, materials science, and chemical engineering. Store in a cool, dry place away from light and moisture to maintain stability.
- CAS No: 13656-61-6
- Molecular Formula: C12H9FO3S
- Molecular Weight: 252.26
- Exact Mass: 252.02564348
- Monoisotopic Mass: 252.02564348
- IUPAC Name: phenyl 4-fluorobenzenesulfonate
- SMILES: C1=CC=C(C=C1)OS(=O)(=O)C2=CC=C(C=C2)F
- Synonyms: 13656-61-6, phenyl 4-fluorobenzenesulfonate, CBMicro_018195, SCHEMBL3792465, DTXSID401305182
Application
Phenyl 4-fluorobenzenesulfonate is widely utilized as a key intermediate in the synthesis of fluorinated aromatic compounds, particularly in pharmaceutical and agrochemical research. It serves as a versatile electrophile in nucleophilic aromatic substitution (SNAr) reactions, enabling the introduction of fluorinated motifs into complex molecules. Researchers also employ it in polymer chemistry to modify sulfonate-containing monomers for advanced material applications. Its stability and reactivity make it a preferred choice for controlled functionalization in multi-step synthetic routes.
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