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tetra-n-butylphosphonium.tetrakis(pentafluorophenyl)borate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

443889-03-0

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443889-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 443889-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,8,8 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 443889-03:
(8*4)+(7*4)+(6*3)+(5*8)+(4*8)+(3*9)+(2*0)+(1*3)=180
180 % 10 = 0
So 443889-03-0 is a valid CAS Registry Number.

443889-03-0Downstream Products

443889-03-0Relevant academic research and scientific papers

Ion pairs of weakly coordinating cations and anions: Synthesis and application for sulfide to sulfoxide oxidations

Zhang, Bo,Li, Su,Cokoja, Mirza,Herdtweck, Eberhardt,Mink, Jnos,Zang, Shu-Liang,Herrmann, Wolfgang A.,Kühn, Fritz E.

, p. 1149 - 1163 (2014)

A series of salts containing the weakly coordinating cations (WCC) 1-butyl-3-methylimidazolium ([Bmim]+), 1-butyl-2,3-dimethylimidazolium ([Bdmim]+), 1-dodecyl-3-methylimidazolium ([C12mim]+), tetrabutylphosphonium ([PBu4]+), tributyltetradecyl

Method for purifying tetrakis(fluoroaryl)borate compounds or tris(fluoroaryl)borate compounds

-

, (2008/06/13)

A solution containing an organic solvent and a compound including impurities, represented by, for example, general formula (1) (wherein R1to R10independently represent H, F, a hydrocarbon group or an alkoxy group, at least one of R1to R5is F, at least one of R6to R10is F, M is H, alkali metal, alkaline earth metal or alkaline earth metal halide, n is 3 or 4, and m is 2 when M is an alkaline earth metal, or m is 1 when M is the other) is mixed with water. The purified compound is reacted with a compound which forms a monovalent cation seed to prepare a derivative. Thus, a purifying method capable of efficiently and easily separating and removing colored components contained in tetrakis(fluoroaryl)borate compounds can be provided. Moreover, it is possible to provide a method capable of preparing a highly-pure tetrakis(fluoroaryl)borate derivative efficiently and at low costs.

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