948043-99-0 Usage
Uses
Used in Pharmaceutical Industry:
4'-Ethyl-3-fluoro-1,1'-biphenyl is used as a building block for the synthesis of various pharmaceuticals due to its unique structure and properties, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 4'-Ethyl-3-fluoro-1,1'-biphenyl serves as a key intermediate in the production of agrochemicals, aiding in the creation of effective pesticides and other agricultural chemicals.
Used in Materials Science:
4'-Ethyl-3-fluoro-1,1'-biphenyl is utilized as a component in the development of new materials, leveraging its chemical properties to enhance material performance in various applications.
Used in Organic Electronics:
4'-Ethyl-3-fluoro-1,1'-biphenyl is used as a starting material in the production of organic electronic materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaics, due to its compatibility with these technologies.
Used in Organic Chemistry:
4'-Ethyl-3-fluoro-1,1'-biphenyl functions as a reagent in organic chemical reactions, facilitating specific transformations and syntheses that are crucial for the preparation of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 948043-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,8,0,4 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 948043-99:
(8*9)+(7*4)+(6*8)+(5*0)+(4*4)+(3*3)+(2*9)+(1*9)=200
200 % 10 = 0
So 948043-99-0 is a valid CAS Registry Number.
948043-99-0Relevant academic research and scientific papers
Synthetic method of directly coupling aryl halide by aromatic hydrocarbon Grignard reagent in the presence of recycled modified palladium-charcoal
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Paragraph 0012; 0013; 0014, (2016/10/08)
The invention provides a synthetic method of directly coupling aryl halide by an aromatic hydrocarbon Grignard reagent. The synthetic method includes performing reflux and water separation of a catalyst Pd/C and an azeotropic organic solvent of non-halogenated hydrocarbon and water, adding an organic phosphine ligand, performing a complexation reaction to obtain a catalyst organic phosphine ligand complexing Pd/C, using aryl halide as an initial material, performing a Grignard reaction at 10-90 DEG C to obtain a Grignard reagent, adding the catalyst, performing a coupled reaction of aryl halide and the Grignard reagent to obtain a coupling aromatic hydrocarbon. The synthetic method uses one-step method, has low synthesis cost, is green and environmental friendly, and is a high-efficiency and clean synthetic technology of coupling aryl halide.
Ethyl- and vinylbenzenes as anti-inflammatory agents
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, (2008/06/13)
A method of treating inflammation in warm-blooded animals, employing an ethyl- or vinylbenzene as the active anti-inflammatory agent.
Ethyl- and vinylbenzenes as antithromobiotic agents
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, (2008/06/13)
A method of treating vascular thrombosis in warmblooded animals, employing an ethyl- or vinylbenzene as the active antithrombotic agent.
