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t-butyl diphenylphosphinoacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

125144-96-9

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125144-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125144-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,1,4 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 125144-96:
(8*1)+(7*2)+(6*5)+(5*1)+(4*4)+(3*4)+(2*9)+(1*6)=109
109 % 10 = 9
So 125144-96-9 is a valid CAS Registry Number.

125144-96-9Downstream Products

125144-96-9Relevant academic research and scientific papers

The hemilabile behaviour of alkyl diphenylphosphinoacetate ligands promoting the reversible coordination of small molecules on (η6-arene)ruthenium(II) centres

Demerseman, Bernard,Renouard, Corinne,Lagadec, Ronan Le,Gonzalez, Marta,Crochet, Pascale,Dixneuf, Pierre H.

, p. 229 - 240 (2007/10/02)

Complexes 6-arene)1-Ph2PCH2C=O)OR>RuCl2> have been prepared.Easy methanolysis and hydrolysis of the ester function occur when R=t-Bu.When R=Me, the stability of the ester function allows the synthesis of the stable salts 6-arene)2-Ph2PCH2C(=O)OMe>RuCl>X (X=PF6 or BF4).Preparation of 6-arene)(L)1-Ph2PCH2C(=O)OMe>RuCl>+ (L=Me2S, MeCN or t-BuCN) from η1-P- and η2-(P,O)-methyl phosphinoacetate derivatives has been studied and the strength of both the L and ester ruthenium coordinative bonds compared.The reactivity of these functional phosphine complexes differs markedly from that of the homologous compounds 6-arene)(PMe3)RuCl2>,6-arene)RuCl2> and 6-arene)2-Ph2PC(R)=C(R')O>RuCl.Competitive and reversible coordination of dimethylsulfide and nitriles or of the ester function is observed and a change in the arene produces selectivity in the coordination of dimethylsulfide and nitriles.Key words: Ruthenium; Iron; Phosphine; Arene

SYNTHESIS OF SOME FUNCTIONALIZED PHOSPHINOCARBOXYLIC ACIDS

van Doorn, J. A.,Meijboom, N.

, p. 211 - 222 (2007/10/02)

Various functionalized phosphinocarboxylic acids have been prepared by a number of complementary methods.Reactions of relatively electron-poor secondary phosphides with electron-rich halocarboxylates in liquid ammonia give high yields of phosphinocarboxylates.The substitution reactionmay proceed by a classical SN2 mechanism or by an SN rad mechanism.Reduction of the carboxilate can be a deleterious side reaction in the preparation of phosphinoacetic acids.Several phosphinopropionic acids are prepared by the Michael adition of diphenylphosphine to unsaturated esters.A valuable method proved to be the reaction of dichlorophosphinoacetic ester with functionalized organometallic reagents. Key words: Phosphine; carboxylic acid; ligand; functionalized; synthesis; NMR data.

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