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1H-Indole-3-carboxylic acid, 2-ethyl-5-methoxy-1-(phenylmethyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

184705-08-6

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184705-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 184705-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,7,0 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 184705-08:
(8*1)+(7*8)+(6*4)+(5*7)+(4*0)+(3*5)+(2*0)+(1*8)=146
146 % 10 = 6
So 184705-08-6 is a valid CAS Registry Number.

184705-08-6Relevant academic research and scientific papers

Synthesis of indomethacin analogues for evaluation as modulators of MRP activity

Maguire, Anita R.,Plunkett, Stephen J.,Papot, Sébastien,Clynes, Martin,O'Connor, Robert,Touhey, Samantha

, p. 745 - 762 (2007/10/03)

Synthesis of a range of indomethacin analogues, required for investigation in combination toxicity assays, bearing both N-benzyl and N-benzoyl groups, is described. Copyright

Controlling the rates of reductively-activated elimination from the (indol-3-yl)methyl position of indolequinones

Everett, Steven A.,Naylor, Matthew A.,Barraja, Paola,Swann, Elizabeth,Patel, Kantilal B.,Stratford, Michael R. L.,Hudnott, Anna R.,Vojnovic, Borivoj,Locke, Rosalind J.,Wardman, Peter,Moody, Christopher J.

, p. 843 - 860 (2007/10/03)

A series of substituted 3-(4-nitrophenyloxy)methylindole-4,7-diones (Q) were synthesised. The effects of substitution patterns on the indole core on rates of elimination of 4-nitrophenol as a model for drug release following fragmentation of a phenolic et

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