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About This Item
Linear Formula:
C6H4(COC6H4F)2
CAS Number:
Molecular Weight:
322.30
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
form
solid
mp
181-183 °C (lit.)
SMILES string
Fc1ccc(cc1)C(=O)c2cccc(c2)C(=O)c3ccc(F)cc3
InChI
1S/C20H12F2O2/c21-17-8-4-13(5-9-17)19(23)15-2-1-3-16(12-15)20(24)14-6-10-18(22)11-7-14/h1-12H
InChI key
PISLKPDKKIDMQT-UHFFFAOYSA-N
General description
1,3-Bis(4-fluorobenzoyl)benzene is an organic building block. It polymerizes with 4,4′-isopropylidenediphenol (bisphenol-A) in the presence of N-methyl-2-pyrrolidinone (solvent) to afford high molecular weight polymers.
Application
1,3-Bis(4-fluorobenzoyl)benzene was used for the synthesis of sulfonated poly(aryl ether ketone)s (SPAEK) copolymers by aromatic nucleophilic polycondensation. It may be employed as an activated nonsulfonated difluoro-monomer for the synthesis of fluorenyl-containing sulfonated poly(aryl ether ether ketone ketone)s.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Find documentation for the products that you have recently purchased in the Document Library.
Fluorenyl-containing sulfonated poly (aryl ether ether ketone ketone) s (SPFEEKK) for fuel cell applications
Li B, et al.
Journal of Membrane Science, 280(1), 54-64 (2006)
Polyimides containing carbonyl and ether connecting groups.
Hergenrother PM, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 25(4), 1093-1103 (1987)
Competing processes for poly (aryl ether-ketone) synthesis, 3. Polymerization reactions of 1, 3-bis (4-chlorobenzoyl) benzene and 1, 3-bis (4-fluorobenzoyl) benzene in N-methyl-2-pyrrolidinone.
Bhatnagar A, et al.
Macromolecular Chemistry and Physics, 197(1), 315-328 (1996)
Macromolecular Chemistry and Physics, 197, 315-315 (1996)
Synthesis and characterization of poly (aryl ether ketone) copolymers containing (hexafluoroisopropylidene)-diphenol moiety as proton exchange membrane materials.
Xing P, et al.
Polymer, 46(10), 3257-3263 (2005)
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