2399-48-6

Basic information

• Product Name: Tetrahydrofurfuryl acrylate
• Synonyms: ACRYLIC ACID TETRAHYDROFURFURYL ESTER;LABOTEST-BB LT00159260;(tetrahydro-2-furanyl)methyl2-propenoate;2-Propenoicacid,(tetrahydro-2-furanyl)methylester;2-Propenoicacid,tetrahydrofurfurylester;kayaradtc101;lightacrylatethf-a;sartomer285
• CAS NO: 2399-48-6
• Molecular Formula: C₈H₁₂O₃
• Molecular Weight: 156.18
• EINECS: 219-268-7
• Product Categories: AcrylateSelf Assembly&Contact Printing;Fluorine-Containing Monomers for 157 nm UV Lithography Resist PolymersBuilding Blocks;Acrylic Monomers;Furans;Heterocyclic Building Blocks;Lithography Monomers;Monomers
• Mol File: 2399-48-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 87 °C9 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 1.064 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.023mmHg at 25°C
• Refractive Index: n20/D 1.46(lit.)
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Soluble in water
• Water Solubility: 79.1g/L at 20.9℃
• BRN: 113115
• CAS DataBase Reference: Tetrahydrofurfuryl acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: Tetrahydrofurfuryl acrylate(2399-48-6)
• EPA Substance Registry System: Tetrahydrofurfuryl acrylate(2399-48-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/38
• Safety Statements: 26
• RIDADR: 3334
• WGK Germany: 3
• RTECS: UD3670893
• TSCA: Yes
• HazardClass: 9
• Hazardous Substances Data: 2399-48-6(Hazardous Substances Data)

Usage

Uses

Tetrahydrofurfuryl acrylate may be used as an acrylic matrix for silver nanoparticles/polymer nanocomposites . It can form copolymers with butadiene. Prior to transfer printing, cellulosic and proteinic fibers are grafted with THFA.

InChI:InChI=1/C8H12O3/c1-2-8(9)11-6-7-4-3-5-10-7/h2,7H,1,3-6H2

Upstream product

• 97-99-4 Tetrahydrofurfuryl alcohol 
• 140-88-5 ethyl acrylate 
• 814-68-6 acryloyl chloride 
• 74-86-2 acetylene 

Downstream Products

• 1428346-04-6 (Z)-(tetrahydrofuran-2-yl)methyl 2-bromo-3-(phenylamino)acrylate 
• 1428346-05-7 (E)-(tetrahydrofuran-2-yl)methyl 2-bromo-3-(phenylamino)acrylate 
• 73172-56-2 ethyl 4-benzoylbutanoate 

Relevant articles and documents

Ruthenium(II) oxidase catalysis for C-H alkenylations in biomass-derived γ-valerolactone

Ruthenium(ii) biscarboxylate oxidase catalysis is a powerful tool for the assembly of functionalized arenes with oxygen as a green oxidant, but this strategy was thus far limited to its use in traditional organic solvents. Herein, we report on a green procedure for the ruthenium(ii) biscarboxylate-catalysed C-H functionalisation in biomass-derived γ-valerolactone as the reaction medium. The oxidase catalysis was characterized by ample substrate scope and proceeded efficiently with oxygen as the sole oxidant. The overall green nature of this C-H-activation methodology is reflected by H2O being the only by-product.