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cinnamyl-phosphinic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1207192-25-3

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1207192-25-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1207192-25-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,1,9 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1207192-25:
(9*1)+(8*2)+(7*0)+(6*7)+(5*1)+(4*9)+(3*2)+(2*2)+(1*5)=123
123 % 10 = 3
So 1207192-25-3 is a valid CAS Registry Number.

1207192-25-3Relevant academic research and scientific papers

DBU-promoted alkylation of alkyl phosphinates and H-phosphonates

Gavara, Laurent,Petit, Christelle,Montchamp, Jean-Luc

supporting information, p. 5000 - 5003 (2012/11/07)

The alkylation of alkyl phosphinates and some H-phosphonate diesters is promoted by the base DBU. Only more reactive alkyl halides react in preparatively useful yields. However, the method provides easy access to important H-phosphinate building blocks, without the need for a protecting group strategy or metal catalysts. The reaction is conveniently conducted at, or below, room temperature. The preparation of methyl-H-phosphinate esters is particularly interesting as it avoids the heretofore more common use of methyldichlorophosphine MePCl2.

Chemistry of the versatile (hydroxymethyl)phosphinyl P(O)CH2OH functional group

Berger, Olivier,Gavara, Laurent,Montchamp, Jean-Luc

supporting information; experimental part, p. 3404 - 3407 (2012/09/08)

(Hydroxymethyl)phosphorus compounds are well-known and valuable compounds in general; however the use of (hydroxymethyl)phosphinates R1P(O) (OR2)CH2OH in particular has been much more limited. The potential of this functio

Facile P,N-heterocycle synthesis via tandem aminomethylation-cyclization of H-phosphinate building blocks

Queffelec, Clemence,Montchamp, Jean-Luc

supporting information; experimental part, p. 267 - 273 (2010/04/24)

Various heterocycles containing phosphorus and nitrogen are easily synthesized from readily available H-phosphinate building blocks. Aminomethylation of these H-phosphinates is followed by in situ cyclization through substitution or cross-coupling to prod

Temporary protection of H-phosphinic acids as a synthetic strategy

Coudray, Laetitia,Montchamp, Jean-Luc

supporting information; experimental part, p. 4646 - 4654 (2009/12/06)

H-Phosphinates obtained through, various methodologies are protected directly by the reaction with triethyl orthoacetate. The resulting products can be manipulated easily, and various synthetic reactions are presented. For example, application to the synt

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