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Quinoline, 4-ethoxy-2-phenyl-, 1-oxide, also known as 2-phenyl-4-ethoxyquinoline 1-oxide, is a chemical compound with the molecular formula C17H15NO2. It is a derivative of quinoline, a heterocyclic aromatic compound with a benzene ring fused to a pyridine ring. The 4-ethoxy-2-phenyl-1-oxide structure indicates the presence of an ethoxy group at the 4-position, a phenyl group at the 2-position, and an oxide group at the 1-position. Quinoline, 4-ethoxy-2-phenyl-, 1-oxide is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical properties and reactivity. It is an important intermediate in the development of new drugs and can also be used as a building block in the creation of more complex organic molecules.

3475-17-0

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3475-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3475-17-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,7 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3475-17:
(6*3)+(5*4)+(4*7)+(3*5)+(2*1)+(1*7)=90
90 % 10 = 0
So 3475-17-0 is a valid CAS Registry Number.

3475-17-0Relevant academic research and scientific papers

ON THE REACTION MECHANISM OF HETEROAROMATIC N-OXIDES WITH 5-HEXENYLMAGNESIUM BROMIDE

Eberson, Lennart,Cardellini, Liberato,Greci, Lucedio,Poloni, Marino

, p. 35 - 40 (2007/10/02)

The reactions of quinoline N-oxide, 1a, 2-cyano-, 1b, and 4-cyano-quinoline N-oxide, 1c, and 2-phenyl-3-phenylimino-3H-indole N-oxide, 9, with 5-hexenylmagnesium bromide have been studied in order to obtain an insight into the reaction mechanism (electron transfer vs. nucleophilic attack).Only the strongest oxidant, i.e. 9 (Ered = -0.74 V vs.NHE), gave any positive indication of an electron-transfer (ET) mechanism, in that a product with partially (20percent) cyclized structure (5-hexenyl to cyclopentylmethyl) could be isolated.

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