Description
Bis[4-[4-amino-2-(trifluoromethyl)phenoxy]phenyl] sulfone (CAS No. 138322-14-2) is a high-purity sulfone-based compound with the molecular formula C26H18F6N2O4S. This specialized chemical features a unique bis-phenoxy sulfone structure with trifluoromethyl and amino functional groups, making it valuable for advanced research and industrial applications. Its IUPAC name is 4-[4-[4-[4-amino-2-(trifluoromethyl)phenoxy]phenyl]sulfonylphenoxy]-3-(trifluoromethyl)aniline. The compound is characterized by its high thermal stability and potential for use in high-performance polymer synthesis, pharmaceutical intermediates, and electronic materials. Available in various quantities with guaranteed purity levels, this product is ideal for researchers requiring precise and reliable chemical building blocks.
Properties
- CAS Number: 138322-14-2
- Complexity: 830
- IUPAC Name: 4-[4-[4-[4-amino-2-(trifluoromethyl)phenoxy]phenyl]sulfonylphenoxy]-3-(trifluoromethyl)aniline
- InChI: InChI=1S/C26H18F6N2O4S/c27-25(28,29)21-13-15(33)1-11-23(21)37-17-3-7-19(8-4-17)39(35,36)20-9-5-18(6-10-20)38-24-12-2-16(34)14-22(24)26(30,31)32/h1-14H,33-34H2
- InChI Key: PBCUJIJENFOTDR-UHFFFAOYSA-N
- Exact Mass: 568.08914721
- Molecular Formula: C26H18F6N2O4S
- Molecular Weight: 568.5
- SMILES: C1=CC(=CC=C1OC2=C(C=C(C=C2)N)C(F)(F)F)S(=O)(=O)C3=CC=C(C=C3)OC4=C(C=C(C=C4)N)C(F)(F)F
- Topological: 113
- Monoisotopic Mass: 568.08914721
- Synonyms: 138322-14-2, Bis[4-[4-amino-2-(trifluoromethyl)phenoxy]phenyl] sulfone, SCHEMBL653313, PBCUJIJENFOTDR-UHFFFAOYSA-N, DTXSID601152317, DB-411786, 4,4′-[Sulfonylbis(4,1-phenyleneoxy)]bis[3-(trifluoromethyl)benzenamine], 4,4a(2)-[Sulfonylbis(4,1-phenyleneoxy)]bis[3-(trifluoromethyl)benzenamine], 4,4′-((Sulfonylbis(4,1-phenylene))bis(oxy))bis(3-(trifluoromethyl)aniline)
Application
Bis[4-[4-amino-2-(trifluoromethyl)phenoxy]phenyl] sulfone is primarily used as a key intermediate in the synthesis of high-performance polymers, particularly polyimides and polyether sulfones, due to its thermally stable sulfone linkage and reactive amino groups. Its trifluoromethyl groups enhance solubility and impart unique electronic properties, making it suitable for advanced material science applications. Researchers also explore its potential in pharmaceutical development as a scaffold for bioactive molecules. The compound’s robust structure lends itself to applications in specialty coatings and adhesives where chemical resistance is critical.
If you are interested or have any questions, please contact us at support@atomfair.com
Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


Reviews
There are no reviews yet.