13642-97-2

Usage

Uses

Used in Chemical Synthesis:
PENTAFLUOROPHENYL METHACRYLATE is used as an activated ester for coupling reactions, such as esterification and amidation. Its reactivity makes it a valuable component in the synthesis of various compounds and materials.
Used in Polymer Industry:
PENTAFLUOROPHENYL METHACRYLATE is used as a monomer for the production of low refractive index polymers, with a refractive index of approximately 1.40. These polymers have potential applications in the optical and electronics industries, where materials with specific refractive properties are required.

InChI:InChI=1/C10H5F5O2/c1-3(2)10(16)17-9-7(14)5(12)4(11)6(13)8(9)15/h1H2,2H3

Upstream product

• 771-61-9 2,3,4,5,6-pentafluorophenol 
• 920-46-7 Methacryloyl chloride 
• 79-41-4 poly(methacrylic acid) 

Downstream Products

• 5438-81-3 3,3-dimethyl-1,4-diphenyl-azetidin-2-one 

Related news

Optical and thermal properties of methyl methacrylate and PENTAFLUOROPHENYL METHACRYLATE (cas 13642-97-2) copolymer: Design of copolymers for low-loss optical fibers for gigabit in-home communications09/07/2019

As a novel base material for low-loss graded index plastic optical fibers (GI POFs) in gigabit home networks, a copolymer of methyl methacrylate (MMA) and pentafluorophenyl methacrylate (PFPMA) was prepared and its thermal and optical properties were investigated. When the PFPMA content in the m...detailed

Relevant academic research and scientific papers

Functional-Polymer Library through Post-Polymerization Modification of Copolymers Having Oleate and Pentafluorophenyl Pendants

Poly[2-(methacryloyloxy)ethyl oleate-co-pentafluorophenyl methacrylate] [P(MAEO-co-PFPMA)] random copolymers with oleate and pentafluorophenyl side-chain pendants were synthesized. These copolymers were utilized as dual-reactive polymeric scaffolds in a range of post-polymerization modification strategies involving thiol-ene and para-fluoro-thiol substitution, amidation, trans-esterification, and epoxidation followed by amidation. The 2-(methacryloyloxy)ethyl oleate (MAEO) functional handle in the copolymer is open to functionalization at its internal double bond through thermally initiated thiol-ene reaction, whereas the pentafluorophenyl moiety of the pentafluorophenyl methacrylate (PFPMA) unit undergoes para-fluoro-thiol substitution under basic conditions at room temperature. By means of these modification approaches, the P(MAEO-co-PFPMA) copolymer was orthogonally ligated with thiol compounds having, for example, alkyl, hydroxyl, and protected amine functional groups. Furthermore, different functional groups such as benzyl, allyl, methacrylate, pyrene, and water-soluble poly(ethylene glycol) were easily introduced into the side chain of the P(MAEO-co-PFPMA) copolymer by amidation, trans-esterification, and epoxidation followed by amidation. Functionalization of both the reactive pendants with the various organic substituents was confirmed by 1H and 19F NMR spectroscopy, gel permeation chromatography, and fluorescence spectroscopy.

Comparison of systematically functionalized heterogeneous and homogenous glycopolymers as toxin inhibitors

Multivalent glycosylated polymers and particles display enhanced binding affinity toward lectins compared to individual glycans. The design of glycopolymers with selectivity toward pathogen-associated lectins (toxins) for sensing or in antiadhesion therap

FORCE-RESPONSIVE POLYMERSOMES AND NANOREACTORS; PROCESSES UTILIZING THE SAME

The mechanically induced melting properties of DNA were employed to achieve force labile membranes is described. Nucleobase pairs were used as mechanophores. Adenine and thymine functionalized complementary amphiphilic block copolymers were self-assembled

Estimation on the optic loss for acrylic polymers by theoretical modification

Various fluorinated/chlorinated polymers were synthesized and characterized by FT-IR and 1H NMR. Also, theoretical optic loss of the POF were investigated and proposed for the purpose of finding a definite rule of the optic loss.From the comput

Process for the preparation of halogenated (meth)acrylic esters and poly (meth) arcylates obtained with said (meth)acrylic esters

The present invention is directed to a process for the preparation of (meth)acrylates of halogenated alcohols by direct esterification of said alcohols with (meth)acrylic acid (chloride) wherein at least 2,6-substituted pyridine derivative is used as a po