51760-04-4 Usage
Uses
Used in Pharmaceutical Industry:
1-Bromo-4-fluoro-2,5-dimethylbenzene is used as a chemical intermediate for the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
1-Bromo-4-fluoro-2,5-dimethylbenzene is used as a chemical intermediate in the production of agrochemicals. It contributes to the development of effective pesticides and other agricultural chemicals to protect crops and enhance agricultural productivity.
Used in Specialty Chemicals Production:
1-Bromo-4-fluoro-2,5-dimethylbenzene is used as a reagent in the production of specialty chemicals. Its versatile chemical properties enable the synthesis of a wide range of specialty chemicals for various applications.
Used in Research Laboratories:
1-Bromo-4-fluoro-2,5-dimethylbenzene is used in research laboratories for various chemical processes and applications. Its unique structure and reactivity make it a valuable compound for scientific investigations and the development of new chemical reactions.
Used in Industrial Settings:
1-Bromo-4-fluoro-2,5-dimethylbenzene is used in industrial settings for various chemical processes and applications. Its versatility as a chemical intermediate and reagent contributes to the production of a wide range of products in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 51760-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,7,6 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51760-04:
(7*5)+(6*1)+(5*7)+(4*6)+(3*0)+(2*0)+(1*4)=104
104 % 10 = 4
So 51760-04-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H8BrF/c1-5-4-8(10)6(2)3-7(5)9/h3-4H,1-2H3
51760-04-4Relevant academic research and scientific papers
REAGENTS AND PROCESS FOR DIRECT C-H FUNCTIONALIZATION
-
Page/Page column 95, (2020/06/01)
Thianthrene derivative of the Formula (I): wherein R1 to R8 may be the same or different and are selected from hydrogen, Cl, F, a partially or fully fluorinated C1 to C6 alkyl group, and wherein n is 0 or 1, with the proviso that at least one of R1 to R8 is not hydrogen and process for C-H functionalization of aromatic compounds using this compound.
Photoredox catalysis with aryl sulfonium salts enables site-selective late-stage fluorination
Li, Jiakun,Chen, Junting,Sang, Ruocheng,Ham, Won-Seok,Plutschack, Matthew B.,Berger, Florian,Chabbra, Sonia,Schnegg, Alexander,Genicot, Christophe,Ritter, Tobias
, p. 56 - 62 (2019/11/28)
Photoredox catalysis, especially in combination with transition metal catalysis, can produce redox states of transition metal catalysts to facilitate challenging bond formations that are not readily accessible in conventional redox catalysis. For arene functionalization, metallophotoredox catalysis has successfully made use of the same leaving groups as those valuable in conventional cross-coupling catalysis, such as bromide. Yet the redox potentials of common photoredox catalysts are not sufficient to reduce most aryl bromides, so synthetically useful aryl radicals are often not directly available. Therefore, the development of a distinct leaving group more appropriately matched in redox potential could enable new reactivity manifolds for metallophotoredox catalysis, especially if arylcopper(iii) complexes are accessible, from which the most challenging bond-forming reactions can occur. Here we show the conceptual advantages of aryl thianthrenium salts for metallophotoredox catalysis, and their utility in site-selective late-stage aromatic fluorination.
