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Phosphonic acid, methyl-, 2-oxo-2-phenylethyl phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41318-92-7

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41318-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41318-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,1 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41318-92:
(7*4)+(6*1)+(5*3)+(4*1)+(3*8)+(2*9)+(1*2)=97
97 % 10 = 7
So 41318-92-7 is a valid CAS Registry Number.

41318-92-7Downstream Products

41318-92-7Relevant academic research and scientific papers

Synthesis of phenyl or 4-nitrophenyl methyl β-ketophosphonate esters

Reddy, Putta M.,Viragh, Carol,Kovach, Ildiko M.

, p. 1597 - 1600 (2007/10/03)

Seven new aryl methyl β-ketophosphonate esters were synthesized. The hydrolytic rates of the compounds under physiological conditions were studied. Most of the compounds are effective inhibitors of acetylcholinesterase. The enzyme recovers on the 10-50 h

New organohypervalent iodine reagents for α-methylphosphonylations and α-diphenyl- and α-dimethylphosphinylations

Moriarty, Robert M.,Condeiu, Cristian,Tao, Anping,Prakash, Om

, p. 2401 - 2404 (2007/10/03)

[Hydroxy(((phenoxy)(methyl)phosphoryl)oxy)iodo]benzene (1), [hydroxy(((diphenyl)phosphoryl)oxy)iodo]benzene (2) and [hydroxy(((dimethyl)phosphoryl)oxy)iodo]benzene (3), obtained from the reaction of iodosobenzene with phenyl methylphosphonic acid, diphenyl- and dimethylphosphinic acid, respectively, effect the introduction of the corresponding phosphonate or phosphinate groups α- to ketone and eater carbonyl groups. Phenylacetylene is transformed by reagents 1-3 into the corresponding α-functionalized acetophenone derivatives.

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