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benzyl 7-(2-bromoethoxy)coumarin-4-acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1226895-46-0

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1226895-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1226895-46-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,6,8,9 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1226895-46:
(9*1)+(8*2)+(7*2)+(6*6)+(5*8)+(4*9)+(3*5)+(2*4)+(1*6)=180
180 % 10 = 0
So 1226895-46-0 is a valid CAS Registry Number.

1226895-46-0Relevant articles and documents

A HTS assay for the detection of organophosphorus nerve agent scavengers

Louise-Leriche, Ludivine,Paunescu, Emilia,Saint-Andre, Geraldine,Baati, Rachid,Romieu, Anthony,Wagner, Alain,Renard, Pierre-Yves

experimental part, p. 3510 - 3523 (2010/07/06)

A new pro-fluorescent probe aimed at a HTS assay of scavengers is able to selectively and efficiently cleave the P-S bond of organophosphorus nerve agents and by this provides non-toxic phosphonic acid has been designed and synthesised. The previously described pro-fluorescent probes were based on a conventional activated P-Oaryl bond cleavage, whereas our approach uses a self-immolative linker strategy that allows the detection of phosphonothioase activity with respect to a non-activated P-Salkyl bond. Further, we have also developed and optimised a high-throughput screening assay for the selection of decontaminants (chemical or biochemical scavengers) that could efficiently hydrolyse highly toxic V-type nerve agents. A preliminary screening, realised on a small α-nucleophile library, allowed us to identify some preliminary "hits", among which pyridinealdoximes, α-oxo oximes, hydroxamic acids and, less active but more original, amidoximes were the most promising. Their selective phosphonothioase activity has been further confirmed by using PhX as the substrate, and thus they offer new perspectives for the synthesis of more potent V nerve agent scavengers.

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