518070-26-3 Usage
Uses
Used in Pharmaceutical Industry:
Benzeneacetonitrile, 2-fluoro-4-methyl(9CI) is utilized as a key intermediate in the synthesis of pharmaceutical compounds. Its unique structural features, including the presence of a fluorine atom and a methyl group, contribute to the development of new drugs with enhanced properties, such as improved bioavailability, selectivity, and potency.
Used in Agrochemical Industry:
In the agrochemical sector, Benzeneacetonitrile, 2-fluoro-4-methyl(9CI) serves as a valuable intermediate for the production of agrochemicals, including pesticides and herbicides. Its reactivity and structural attributes enable the creation of novel compounds with increased effectiveness and selectivity, contributing to more efficient and sustainable agricultural practices.
Used in Organic Synthesis:
Benzeneacetonitrile, 2-fluoro-4-methyl(9CI) is employed as a versatile building block in organic synthesis. Its fluorinated and methylated functional groups allow for the development of a wide range of organic compounds with diverse applications, such as in materials science, pharmaceuticals, and agrochemicals. Benzeneacetonitrile, 2-fluoro-4-methyl(9CI)'s reactivity and structural features facilitate the synthesis of complex molecules with specific properties and functions.
Check Digit Verification of cas no
The CAS Registry Mumber 518070-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,8,0,7 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 518070-26:
(8*5)+(7*1)+(6*8)+(5*0)+(4*7)+(3*0)+(2*2)+(1*6)=133
133 % 10 = 3
So 518070-26-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8FN/c1-7-2-3-8(4-5-11)9(10)6-7/h2-3,6H,4H2,1H3
518070-26-3Relevant articles and documents
Synthesis of α-Aryl nitriles through palladium-catalyzed decarboxylative coupling of cyanoacetate salts with aryl halides and triflates
Shang, Rui,Ji, Dong-Sheng,Chu, Ling,Fu, Yao,Liu, Lei
supporting information; experimental part, p. 4470 - 4474 (2011/06/24)
Worth its salt: The palladium-catalyzed decarboxylative coupling of the cyanoacetate salt as well as its mono- and disubstituted derivatives with aryl chlorides, bromides, and triflates is described (see scheme). This reaction is potentially useful for the preparation of a diverse array of α-aryl nitriles and has good functional group tolerance. S-Phos=2-(2,6- dimethoxybiphenyl)dicyclohexylphosphine), Xant-Phos=4,5-bis(diphenylphosphino)- 9,9-dimethylxanthene. Copyright
