948043-99-0

Basic information

• Product Name: 4'-Ethyl-3-fluoro-1,1'-biphenyl
• Synonyms: 4'-Ethyl-3-fluoro-1,1'-biphenyl;4'-Ethyl-3-fluorobiphenyl;1-ethyl-4-(3-fluorophenyl)benzene
• CAS NO: 948043-99-0
• Molecular Formula: C14H13F
• Molecular Weight: 200.2514232
• EINECS: 918-150-9
• Mol File: 948043-99-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 289.7±19.0 °C(Predicted)
• Appearance: /
• Density: 1.044±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4'-Ethyl-3-fluoro-1,1'-biphenyl(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-Ethyl-3-fluoro-1,1'-biphenyl(948043-99-0)
• EPA Substance Registry System: 4'-Ethyl-3-fluoro-1,1'-biphenyl(948043-99-0)

Safety Data

• Hazardous Substances Data: 948043-99-0(Hazardous Substances Data)

Usage

General Description

4'-Ethyl-3-fluoro-1,1'-biphenyl is a chemical compound that consists of a biphenyl core with an ethyl group and a fluorine atom attached to specific positions of the molecule. It is a colorless liquid at room temperature and is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and materials. 4'-Ethyl-3-fluoro-1,1'-biphenyl is also utilized as a starting material in the production of organic electronic materials and as a reagent in organic chemical reactions. Its unique structure and properties make it a valuable intermediate in the manufacturing of a wide range of products and materials.

Relevant articles and documents

Synthetic method of directly coupling aryl halide by aromatic hydrocarbon Grignard reagent in the presence of recycled modified palladium-charcoal

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 antithromobiotic agents

A method of treating vascular thrombosis in warmblooded animals, employing an ethyl- or vinylbenzene as the active antithrombotic agent.