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henicosafluorodecyldiphenylphosphine sulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1424372-91-7

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1424372-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1424372-91-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,4,3,7 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1424372-91:
(9*1)+(8*4)+(7*2)+(6*4)+(5*3)+(4*7)+(3*2)+(2*9)+(1*1)=147
147 % 10 = 7
So 1424372-91-7 is a valid CAS Registry Number.

1424372-91-7Downstream Products

1424372-91-7Relevant academic research and scientific papers

PHOSPHINE COMPOUND HAVING PERFLUORO GROUP, AND COMPLEX BETWEEN METAL AND PHOSPHINE HAVING PERFLUORO GROUP

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, (2018/10/16)

PROBLEM TO BE SOLVED: To provide a perfluoroalkylphosphine compound, and a complex between a metal and the perfluoroalkylphosphine. SOLUTION: A perfluoroalkylphosphine compound is a phosphine compound represented by the general formula Rf-PR1R2. In the formula, R1 and R2 are each independently a substituted or unsubstituted hydrocarbon group; Rf is a perfluorinated hydrocarbon group. Also provided is a complex between the perfluoroalkylphosphine and a phosphine coordination metal. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

METHODS OF PRODUCING PHOSPHINE COMPOUND HAVING PERFLUORO GROUP AND COMPLEX BETWEEN METAL AND PHOSPHINE HAVING PERFLUORO GROUP

-

, (2018/10/19)

PROBLEM TO BE SOLVED: To provide methods of producing a perfluoroalkylphosphine compound improved in a phosphorus element yield and a chemical yield. SOLUTION: A method of producing a perfluoroalkylphosphine compound comprises either reacting a perfluoroalkyl iodide with, e.g., 2,4,6-trimethylbenzoyldiphenylphosphine oxide (TMDPO) or a triarylphosphine such as triphenylphosphine, which are easily available, in the presence of a radical generator such as azobis(isobutyronitrile) or light irradiation, or reacting TMDPO or the like with perfluoroalkyl iodide in the presence of diphenylphosphine, diethylphosphine, dicyclohexylphosphine or the like. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

Synthesis and properties of perfluoroalkyl phosphine ligands: Photoinduced reaction of diphosphines with perfluoroalkyl iodides

Kawaguchi, Shin-Ichi,Minamida, Yoshiaki,Ohe, Takashi,Nomoto, Akihiro,Sonoda, Motohiro,Ogawa, Akiya

, p. 1748 - 1752 (2013/04/10)

A 'F'lurry of activity: The title reaction provides a convenient procedure for direct synthesis of perfluoroalkylated phosphines. The synthesized phosphine n-C10F21PPh2 forms a complex with palladium(II) to give 1 and several runs of coupling reactions are attained with n-C10F21PPh2 by using a fluorous/organic biphasic system. Copyright

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