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methyl 4-(4-chlorophenyl)-6-methoxyquinoline-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

906463-88-5

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906463-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 906463-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,4,6 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 906463-88:
(8*9)+(7*0)+(6*6)+(5*4)+(4*6)+(3*3)+(2*8)+(1*8)=185
185 % 10 = 5
So 906463-88-5 is a valid CAS Registry Number.

906463-88-5Downstream Products

906463-88-5Relevant academic research and scientific papers

Double-Oxidative Dehydrogenative (DOD) [4 + 2]-Cyclization/Oxidative Aromatization Tandem Reaction of Glycine Derivatives with Ethylbenzenes

Jiang, Wei,Wang, Yajun,Niu, Pengfei,Quan, Zhengjun,Su, Yingpeng,Huo, Congde

supporting information, p. 4649 - 4653 (2018/08/07)

The double-oxidative dehydrogenative (DOD) cyclization represents one of the most straightforward and atom-economical methods for cyclic structure formation. A Cu(II)/DDQ/O2 system-catalyzed DOD [4 + 2]-annulation/oxidative aromatization tandem reaction of readily available glycine derivatives and alkylbenzenes was established. This approach facilitates rapid access to a broad scope of substituted quinoline-2-carboxylate derivatives, an important motif in drug discovery. The reaction could feasibly be applied to a 10 gram-scale synthesis.

Method for synthesizing quinoline compounds through double-oxidation dehydrocyclization reaction

-

Paragraph 0017; 0018; 0034; 0035, (2018/09/21)

The invention provides a method for synthesizing quinoline compounds through a double-oxidation dehydrocyclization reaction. The method comprises the following steps: with N-arylglycine derivatives, ethylbenzene and derivatives thereof as raw materials, copper salt as a catalyst and DDQ as a dehydrogenating agent, reacting at 60-90 DEG C for 5-18 hours under the action of an oxidant; after completion of reaction, performing column chromatography separation to obtain target products. By the method, reaction reagents are low in price and easy to obtain, reaction steps are simple and short, a synthesis condition is mild, the reaction speed is high, the reaction yield is relatively high, the product purity is good, posttreatment is simple and convenient and the industrial production cost can be effectively reduced; therefore, the method is suitable for industrial production.

An efficient route to quinolines and other compounds by iron-catalysed cross-dehydrogenative coupling reactions of glycine derivatives

Liu, Peng,Wang, Zhiming,Lin, Jue,Hu, Xianming

experimental part, p. 1583 - 1589 (2012/05/04)

A simple method has been developed for functionalizing glycine derivatives by iron-catalysed cross-dehydrogenative coupling (CDC) reactions. In particular, N-arylglycine derivatives reacted with alkynes by oxidative C-H/C-H coupling reactions to provide a

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