2399-48-6 Usage
Description
Tetrahydrofurfuryl acrylate (THFA) is a chemical compound derived from tetrahydrofuran and acrylic acid. It is known for its ability to form copolymers and has various applications in different industries due to its unique properties.
Uses
Used in Nanotechnology:
Tetrahydrofurfuryl acrylate is used as an acrylic matrix for silver nanoparticles/polymer nanocomposites. This application takes advantage of THFA's ability to form copolymers, which can enhance the properties of the nanocomposites and improve their performance in various applications.
Used in Polymer Chemistry:
Tetrahydrofurfuryl acrylate is used as a monomer to form copolymers with butadiene. The resulting copolymers can have improved properties, such as increased strength and flexibility, making them suitable for a wide range of applications in the polymer industry.
Used in Textile Industry:
Tetrahydrofurfuryl acrylate is used for grafting cellulosic and proteinic fibers prior to transfer printing. The grafting process involves attaching THFA to the fibers, which can improve their compatibility with other materials and enhance their performance in the printing process.
Check Digit Verification of cas no
The CAS Registry Mumber 2399-48-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,9 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2399-48:
(6*2)+(5*3)+(4*9)+(3*9)+(2*4)+(1*8)=106
106 % 10 = 6
So 2399-48-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O3/c1-2-8(9)11-6-7-4-3-5-10-7/h2,7H,1,3-6H2
2399-48-6Relevant articles and documents
Ruthenium(II) oxidase catalysis for C-H alkenylations in biomass-derived γ-valerolactone
Bechtoldt, Alexander,Baumert, Marcel E.,Vaccaro, Luigi,Ackermann, Lutz
supporting information, p. 398 - 402 (2018/02/07)
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.
