284472-92-0 Usage
Description
TRIS[4-(PERFLUOROOCTYL)PHENYL]PHOSPHINE is a complex organic compound with the chemical formula C24H12F21P. It is a type of triarylphosphine, which is characterized by the presence of three aryl groups attached to a central phosphorus atom. This specific compound features a perfluorooctyl group attached to one of the aryl groups, which may contribute to its unique properties and applications.
Uses
Used in Chemical Synthesis:
TRIS[4-(PERFLUOROOCTYL)PHENYL]PHOSPHINE is used as a reactant for the synthesis of various compounds, including triarylphosphine selenides and perfluoroalkylated arylphosphines. These synthesized products can have a wide range of applications in different industries, such as pharmaceuticals, materials science, and electronics.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, TRIS[4-(PERFLUOROOCTYL)PHENYL]PHOSPHINE is used as a reactant for the synthesis of various drug molecules. Its unique structure and properties make it a valuable building block for the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Materials Science:
In materials science, TRIS[4-(PERFLUOROOCTYL)PHENYL]PHOSPHINE is used as a reactant for the synthesis of advanced materials with specific properties, such as improved thermal stability, chemical resistance, or electrical conductivity. These materials can be utilized in various applications, including aerospace, automotive, and electronics industries.
Used in Electronics Industry:
In the electronics industry, TRIS[4-(PERFLUOROOCTYL)PHENYL]PHOSPHINE is used as a reactant for the synthesis of materials with specific electronic properties, such as semiconductors or conductive polymers. These materials can be used in the development of advanced electronic devices, such as solar cells, sensors, or transistors.
Used in Catalysts:
TRIS[4-(PERFLUOROOCTYL)PHENYL]PHOSPHINE can also be used as a catalyst in various chemical reactions, such as Suzuki coupling and Stille coupling. These coupling reactions are important for the synthesis of complex organic molecules, which can be used in the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 284472-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,4,4,7 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 284472-92:
(8*2)+(7*8)+(6*4)+(5*4)+(4*7)+(3*2)+(2*9)+(1*2)=170
170 % 10 = 0
So 284472-92-0 is a valid CAS Registry Number.
InChI:InChI=1/C42H12F51P/c43-19(44,22(49,50)25(55,56)28(61,62)31(67,68)34(73,74)37(79,80)40(85,86)87)13-1-7-16(8-2-13)94(17-9-3-14(4-10-17)20(45,46)23(51,52)26(57,58)29(63,64)32(69,70)35(75,76)38(81,82)41(88,89)90)18-11-5-15(6-12-18)21(47,48)24(53,54)27(59,60)30(65,66)33(71,72)36(77,78)39(83,84)42(91,92)93/h1-12H
284472-92-0Relevant articles and documents
New approaches to fluorinated ligands and their application in catalysis
Chen, Weiping,Xu, Lijin,Hu, Yulai,Banet Osuna, Anna M,Xiao, Jianliang
, p. 3889 - 3899 (2007/10/03)
Simple and generic approaches to fluorous soluble ligands have been developed and applied to the synthesis of various fluorinated arylphosphines including polymeric ones. The utility of some of these ligands has been demonstrated in catalysis in supercritical CO2 (scCO2) and fluorous solvents.
Novel and efficient synthesis of perfluoroalkylated arylphosphines
Chen, Weiping,Xiao, Jianliang
, p. 3697 - 3700 (2007/10/03)
A novel, high-yield route has been developed for the synthesis of perfluoroalkylated arylphosphines, involving simple, copper-mediated coupling of haloarylphosphine oxides with perfluoroalkyl iodides followed by reduction with trichlorosilane. (C) 2000 Elsevier Science Ltd.
