117358-52-8 Usage
Uses
Used in Adhesives Industry:
1-Ethyl-3,5-difluorobenzene is used as a solvent for adhesives, providing a low-volatility and high-solvency solution that enhances the performance and durability of adhesive formulations.
Used in Coatings Industry:
In the coatings industry, 1-Ethyl-3,5-difluorobenzene is utilized as a solvent to improve the flow and application properties of coatings, contributing to a smoother and more even finish.
Used in Inks Industry:
1-Ethyl-3,5-difluorobenzene is employed as a solvent in inks to ensure proper flow and dispersion of pigments, leading to vibrant colors and consistent print quality.
Used in Pharmaceutical Production:
1-Ethyl-3,5-difluorobenzene is used in the production of pharmaceuticals, where it serves as a chemical intermediate, aiding in the synthesis of various medicinal agents.
Used in Agrochemical Production:
1-Ethyl-3,5-difluorobenzene is also utilized in the agrochemical sector, where it plays a role in the synthesis of compounds used in crop protection and pest management.
Used in Fragrance Industry:
In the fragrance industry, this chemical is used as a solvent or intermediate in the creation of scent compounds, contributing to the development of new and complex fragrances.
It is crucial to handle 1-Ethyl-3,5-difluorobenzene with care due to its potential hazards if inhaled, swallowed, or in contact with skin. Adherence to proper safety precautions and handling procedures is essential when working with 1-Ethyl-3,5-difluorobenzene.
Check Digit Verification of cas no
The CAS Registry Mumber 117358-52-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,3,5 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 117358-52:
(8*1)+(7*1)+(6*7)+(5*3)+(4*5)+(3*8)+(2*5)+(1*2)=128
128 % 10 = 8
So 117358-52-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H8F2/c1-2-6-3-7(9)5-8(10)4-6/h3-5H,2H2,1H3
117358-52-8Relevant academic research and scientific papers
Practical synthesis of optically active fluorine-substituted α-phenylethylamines by retardation of hydrogenolytic cleavage at benzylic position
Kanai, Masatomi,Yasumoto, Manabu,Kuriyama, Yokusu,Inomiya, Kenjin,Katsuhara, Yutaka,Higashiyama, Kimio,Ishii, Akihiro
, p. 1424 - 1425 (2007/10/03)
High regioselectivity in hydrogenolysis of bis(α-methylbenzyl)amines having a fluorine atom on aromatic ring results from retardation of hydrogenolytic cleavage at benzylic position of fluorine-substituted aromatic ring.
