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6-Quinolinecarboxylic acid, 2,4-diphenyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138432-75-4

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138432-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138432-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,3 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138432-75:
(8*1)+(7*3)+(6*8)+(5*4)+(4*3)+(3*2)+(2*7)+(1*5)=134
134 % 10 = 4
So 138432-75-4 is a valid CAS Registry Number.

138432-75-4Downstream Products

138432-75-4Relevant academic research and scientific papers

Quinoline compound and synthesis method thereof

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Paragraph 0131-0135, (2020/02/14)

The invention discloses a synthesis method of a quinoline compound. The synthesis method comprises the following steps: adding a diazocarbonyl compound and a 2-vinylaniline compound into a solvent, carrying out a reaction under the protection of an inert

A multicomponent reaction of acetals for the preparation of quinolines

Zhang, Xue-Lin,Wu, Qin-Pei,Zhang, Qing-Shan

, p. 677 - 680 (2014/01/17)

A straightforward, mild, one-pot method has been found for the preparation of quinolines via a multi-component reaction using acetals or cyclic acetals, aromatic amines and alkynes catalysed by Bi(OTf)3. It gives good yields under mild conditions. This approach has been successfully applied for the synthesis of a range of quinolines with a variety of functional groups.

Annulation Reactions with Iron(III) Chloride: Oxidation of Imines

Leardini, Rino,Nanni, Daniele,Tundo, Antonio,Zanardi, Giuseppe,Ruggieri, Fabrizio

, p. 1842 - 1848 (2007/10/02)

Aromatic imines react with phenylacetylene or styrene in an acetonitrile solution of iron(III) chloride to give quinolines 3 or their tetrahydro derivatives 11 together with variable amounts of products 4 arising from the reduction of the imines.The initial step appears to be a one-electron oxidation to generate iron(II) and an imine radical cation.When the reactions are carried out in the presence of stoichiometric amounts of tetrachloro-p-benzoquinone (chloranil), only quinolines 3 are obtained.

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