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(1-(benzyloxycarbonylamino)-3-methylbutyl)methylphosphinic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119012-11-2

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119012-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119012-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,0,1 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 119012-11:
(8*1)+(7*1)+(6*9)+(5*0)+(4*1)+(3*2)+(2*1)+(1*1)=82
82 % 10 = 2
So 119012-11-2 is a valid CAS Registry Number.

119012-11-2Downstream Products

119012-11-2Relevant academic research and scientific papers

A general method for the synthesis of N-protected α-aminoalkylphosphinic acids

Chen, Shoujun,Coward, James K.

, p. 4335 - 4338 (1996)

A general and highly convenient method for the synthesis of N-protected α-aminophosphinic acids, suitable for side chain elongation either from N-, P-, or C- termini to form a variety of phosphinic peptides, has been developed. The desired phosphinic acids were obtained in moderate to satisfactory yield by a three-component condensation reaction of benzyl carbamate, an aldehyde, and an alkylphosphonous acid (or its 1-adamantanamine salt) in acetyl chloride under very mild conditions.

Arbuzov-type reaction of acylphosphonites and N-alkoxycarbonylimine cations generated in situ with trifluoroacetic anhydride

Dmitriev, Maxim E.,Ragulin, Valery V.

supporting information; experimental part, p. 1634 - 1636 (2012/04/10)

A mild procedure for the synthesis of N-protected α- aminoalkylphosphinic acids by the reaction of N,N′-benzylidene- or N,N′-alkylidenebiscarbamates, trifluoroacetic anhydride and the corresponding alkylphosphonous acids in methylene chloride or toluene i

Amidoalkylation of hydrophosphoryl compounds

Dmitriev,Rossinets,Ragulin

, p. 1092 - 1104 (2011/10/17)

A new mild procedure of the amidoalkylation of hydrophosphoryl compounds in a mixture of acetic anhydride and acetyl chloride was developed as a convenient method of constructing the a-aminophosphoryl fragment of the pseudo-a,a'-dipeptide molecule. The reaction intermediates N,N'-benzylidene- and N,N'-alkylidenebiscarbamates were detected, isolated, and identified. The report presents the results of studying the direct interaction of hydrophosphoryl compounds previously synthesized with biscarbamates in acetic anhydride and other solvents, the influence of the structure of phosphorus component and biscarbamate, and the effect of acid catalysis on the course of this two-component reaction. A new version of the mechanism of the three-component reaction of amidoalkylation of hydrophosphoryl compounds is suggested: it is regarded as a multistage process involving the stage of biscarbamate formation followed by the stage of Arbuzov-type reaction with the intermediate formation of acyliminium cation and P-OAc derivative with trivalent phosphorus. Pleiades Publishing, Ltd., 2011.

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