57469-07-5 Usage
Uses
Used in Adhesive and Crosslinking Applications:
[[2-[p-(oxiranylmethoxy)benzyl]phenoxy]methyl]oxirane is used as a crosslinking agent and adhesive due to the reactivity of its oxirane rings. These groups can form strong covalent bonds with other molecules, making it suitable for various industrial applications where adhesion and crosslinking are required.
Used in Materials Science and Polymer Chemistry:
In the field of materials science and polymer chemistry, [[2-[p-(oxiranylmethoxy)benzyl]phenoxy]methyl]oxirane is used as a building block for creating new materials with specific properties. The presence of multiple reactive groups in its structure allows for the development of novel materials with tailored characteristics, such as enhanced mechanical strength, thermal stability, or chemical resistance.
Used in Coatings and Paints Industry:
[[2-[p-(oxiranylmethoxy)benzyl]phenoxy]methyl]oxirane is used as a component in the formulation of coatings and paints. Its reactive oxirane groups can improve the adhesion, durability, and chemical resistance of the final product, making it a valuable addition to the coatings and paints industry.
Used in Electronics and Semiconductor Industry:
In the electronics and semiconductor industry, [[2-[p-(oxiranylmethoxy)benzyl]phenoxy]methyl]oxirane can be used as a material for the development of advanced encapsulants, adhesives, or coatings. Its reactivity and potential to form strong bonds with other molecules make it a promising candidate for applications where high performance and reliability are crucial.
Check Digit Verification of cas no
The CAS Registry Mumber 57469-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,6 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57469-07:
(7*5)+(6*7)+(5*4)+(4*6)+(3*9)+(2*0)+(1*7)=155
155 % 10 = 5
So 57469-07-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H20O4/c1-2-4-19(23-13-18-12-22-18)15(3-1)9-14-5-7-16(8-6-14)20-10-17-11-21-17/h1-8,17-18H,9-13H2
57469-07-5Relevant academic research and scientific papers
Well-Defined Networks from DGEBF - The Importance of Regioisomerism in Epoxy Resin Networks
Knox, Stephen T.,Wright, Anthony,Cameron, Colin,Fairclough, John Patrick Anthony
, p. 6861 - 6867 (2019/10/02)
The previously ignored or unreported impact of regiosomerism within diglycidyl ether of bisphenol F (DGEBF) on its network properties is presented. Routes to the isomers of DGEBF were explored: high-performance liquid chromatography showed good separation of the three isomers [para-para-DGEBF (ppDGEBF), para-ortho-DGEBF (poDGEBF), and ortho-ortho-DGEBF (ooDGEBF)] with small yields; column chromatography gave good separation of pp- + po- from oo-DGEBF but pp-/po- separation was not achieved. Synthesis was optimized to crude yields of 76% for pp-; 87% for po-, and 86% for oo-. Subsequently, crosslinked networks were prepared with meta-xylylenediamine. With increasing ortho content, degradation of chemical resistance and an inherent weakening of the network was observed, that is, glass transition temperature (Tg), beta transition temperature (Tβ), density, crosslink density, and the desorption diffusion coefficient decreased, whereas sorption diffusion coefficient and ultimate solvent uptake increased. This clearly shows that a subtle chemical structure change can significantly impact network performance.
