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1(2H)-Isoquinolinone, 4-iodo-2,3-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

809274-70-2

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809274-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 809274-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,9,2,7 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 809274-70:
(8*8)+(7*0)+(6*9)+(5*2)+(4*7)+(3*4)+(2*7)+(1*0)=182
182 % 10 = 2
So 809274-70-2 is a valid CAS Registry Number.

809274-70-2Relevant academic research and scientific papers

Construction of isoquinolin-1(2H)-ones by copper-catalyzed tandem reactions of 2-(1-Alkynyl)benzaldimines with water

Zhang, Mingliang,Zhang, Hui-Jun,Ruan, Wenqing,Wen, Ting-Bin

supporting information, p. 5914 - 5918 (2015/09/22)

The Cu(OAc)2-catalyzed tandem reaction of 2-(1-alkynyl)benzaldimines with water for the synthesis of isoquinolin-1(2H)-ones was developed. Moreover, 4-halogen-substituted isoquinolin-1(2H)-ones were obtained in good yields simply by including N-halosuccinimides (NXS: X = Cl, Br, I) in the reaction system. Mechanistic studies indicated that the reactions are probably initiated by highly regioselective intramolecular cyclization of 2-(1-alkynyl)benzaldimines to give the corresponding isoquinolinium intermediates. The Cu(OAc)2-catalyzed tandem reaction of 2-(1-alkynyl)benzaldimines with water for the synthesis of isoquinolin-1(2H)-ones is developed. 4-Halogen-substituted isoquinolin-1(2H)-ones can be obtained in good yields simply by including N-halosuccinimides (NXS) in the reaction system. Mechanistic studies are also undertaken.

Regio- and stereoselective synthesis of isoindolin-1-ones via electrophilic cyclization

Yao, Tuanli,Larock, Richard C.

, p. 1432 - 1437 (2007/10/03)

(Chemical Equation Presented) A variety of substituted isoindolin-1-ones are readily prepared in good to excellent yields under very mild reaction conditions by the reaction of o-(1-alkynyl)benzamides with ICl, I2, and NBS. In a few cases, subs

Synthesis of fused polycycles by 1,4-palladium migration chemistry

Huang, Qinhua,Campo, Marino A.,Yao, Tuanli,Tian, Qingping,Larock, Richard C.

, p. 8251 - 8257 (2007/10/03)

Novel palladium migration/arylation methodology for the synthesis of complex fused polycycles has been developed, in which one or more sequential Pd-catalyzed intramolecular migration processes involving C-H activation are employed. The chemistry works best with electron-rich aromatics, which is in agreement with the idea that these palladium-catalyzed C-H activation reactions parallel electrophilic aromatic substitution.

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