19070-63-4

Usage

Uses

Used in Adhesives Industry:
2-[(2,3-epoxypropoxy)methyl]tetrahydrofuran is used as a monomer for the production of epoxy resins, which are essential in creating high-performance adhesives. These adhesives are valued for their strong bonding capabilities and resistance to various environmental factors.
Used in Coatings Industry:
In the coatings industry, 2-[(2,3-epoxypropoxy)methyl]tetrahydrofuran serves as a key component in the formulation of epoxy resins. These resins contribute to the development of durable and protective coatings with excellent adhesion, chemical resistance, and mechanical properties.
Used in Industrial Applications:
2-[(2,3-epoxypropoxy)methyl]tetrahydrofuran is used as a monomer in various industrial applications, where its reactivity and crosslinking ability are crucial for the production of high-quality polymers and resins. These polymers find use in a wide range of products, from electrical insulation to composite materials.
Used as a Solvent:
2-[(2,3-epoxypropoxy)methyl]tetrahydrofuran is also utilized as a solvent in certain chemical processes, taking advantage of its ability to dissolve a variety of substances and facilitate reactions.
Used as an Intermediate:
2-[(2,3-epoxypropoxy)methyl]tetrahydrofuran acts as an intermediate in the synthesis of specialty chemicals, where it can be further reacted or modified to produce a range of valuable end products.
Used in the Production of Specialty Chemicals:
It is employed in the production of specialty chemicals, where its unique properties can be harnessed to create tailored compounds for specific applications, such as in the pharmaceutical or materials science industries.
It is important to handle 2-[(2,3-epoxypropoxy)methyl]tetrahydrofuran with care, as it may cause irritation to the skin, eyes, and respiratory system if not properly managed.

InChI:InChI=1/C8H14O3/c1-2-7(10-3-1)4-9-5-8-6-11-8/h7-8H,1-6H2/t7-,8-/m1/s1

Upstream product

• 5380-87-0 2-[(2,3-epoxypropoxy)methyl]furan 
• 97-99-4 Tetrahydrofurfuryl alcohol 
• 106-89-8 epichlorohydrin 

Relevant academic research and scientific papers

ACIDIC GROUP-CONTAINING POLYMERIZABLE MONOMER HAVING FUNCTIONAL GROUP HAVING HIGH DIELECTRIC RATE

PROBLEM TO BE SOLVED: To provide an acidic group-containing polymerizable monomer high in compatibility with a polymerizable monomer or the like having an acidic group yet having no acidic group, and having in compatibility with a polymerizable monomer or the like having no acidic group when becoming a salt compound. SOLUTION: There is provided a polymerizable monomer represented by the following general formula (1). In the general formula (1), L is a bivalent hydrocarbon group having at least one monovalent or bivalent functional group derived from a compound X with specific inductive capacity of 5 or more and 5 to 20 carbon atoms, Y represents -O- or -NR2-, wherein R2 is a hydrogen atom or an alkyl group with 1 to 10 carbon atoms. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

Transition metal nanoparticles stabilized by ammonium salts of hyperbranched polystyrene: effect of metals on catalysis of the biphasic hydrogenation of alkenes and arenes

Abstract Hyperbranched polystyrene bearing ammonium salts (HPS-NR3+Cl-) behaves as an excellent stabilizer of ruthenium, rhodium, iridium, palladium, and platinum nanoparticles from 1 to 3 nm in size uniformly dispersed in the polymer matrix. The catalytic performance of the resulting metal-polymer composites, M@HPS-NR3+Cl-, is dependent on the metal. This dependence was investigated by assessing the hydrogenation of alkenes and arenes. The utility of M@HPS-NR3+Cl- as reusable catalysts in aqueous/organic biphasic systems was demonstrated by examining the catalysis of the hydrogenation of aromatic compounds containing various functional groups by Ru@HPS-NR3+Cl-.

Rhodium nanoparticles supported on carbon nanofibers as an arene hydrogenation catalyst highly tolerant to a coexisting epoxido group

Rhodium nanoparticles supported on a carbon nanofiber (Rh/CNF-T) show high catalytic activity toward arene hydrogenation under mild conditions in high turnover numbers without leaching the Rh species; the reaction is highly tolerant to epoxido groups, which often undergo ring-opening hydrogenation with conventional catalysts.