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2H-Indol-2-one, 3-ethoxy-1,3-dihydro-1,3-dimethyl-(9CI) is a chemical compound with the molecular formula C12H15NO2. It belongs to the class of organic compounds known as indolones, which are derivatives of indole with a ketone group at the 2-position. This specific compound features a 3-ethoxy group and two methyl groups attached to the 1 and 3 positions of the indolone core. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those with potential applications in the treatment of neurological disorders and as plant growth regulators. The compound's unique structure and properties make it a valuable building block in the development of new drugs and other chemical products.

503306-62-5

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503306-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 503306-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,3,0 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 503306-62:
(8*5)+(7*0)+(6*3)+(5*3)+(4*0)+(3*6)+(2*6)+(1*2)=105
105 % 10 = 5
So 503306-62-5 is a valid CAS Registry Number.

503306-62-5Downstream Products

503306-62-5Relevant academic research and scientific papers

Reaction of indolin-2-ones with cerium(IV) ammonium nitrate

Escolano, Carmen,Vallverdú, Lluís,Jones, Keith

, p. 9541 - 9545 (2002)

The reaction of indolin-2-ones with CAN is studied. When the reaction is carried out in an alcohol as solvent, 3-alkoxyindolin-2-ones are obtained in very good yields. If a non-nucleophilic solvent is used (THF, acetonitrile) 3-nitroxy derivatives are isolated. If the aromatic ring bears an electron-donating group, reactions are accompanied by aromatic ring nitration.

Electrochemical Umpolung C-H Functionalization of Oxindoles

Pastor, Miryam,Vayer, Marie,Weinstabl, Harald,Maulide, Nuno

, p. 606 - 612 (2022/01/12)

Herein, we present a general electrochemical method to access unsymmetrical 3,3-disubstituted oxindoles by direct C-H functionalization where the oxindole fragment behaves as an electrophile. This Umpolung approach does not rely on stoichiometric oxidants and proceeds under mild, environmentally benign conditions. Importantly, it enables the functionalization of these scaffolds through C-O, and by extension to C-C or even C-N bond formation.

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