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2-([1,1′-biphenyl]-2-yl)isoindolin-1-one is a complex organic compound with the molecular formula C20H13NO. It is a derivative of isoindolin-1-one, featuring a biphenyl group attached to the 2-position of the isoindolinone ring. 2-([1,1′-biphenyl]-2-yl)isoindolin-1-one is known for its potential applications in the field of materials science, particularly as a building block for the synthesis of various functional materials and dyes. Its chemical structure endows it with unique electronic and optical properties, making it a subject of interest for researchers exploring novel compounds with specific characteristics. The compound's synthesis and applications are areas of ongoing study, with potential implications in the development of advanced materials and chemical technologies.

57877-22-2

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57877-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57877-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,7 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57877-22:
(7*5)+(6*7)+(5*8)+(4*7)+(3*7)+(2*2)+(1*2)=172
172 % 10 = 2
So 57877-22-2 is a valid CAS Registry Number.

57877-22-2Downstream Products

57877-22-2Relevant academic research and scientific papers

Site-Selective Ruthenium-Catalyzed C-H Bond Arylations with Boronic Acids: Exploiting Isoindolinones as a Weak Directing Group

Yuan, Yu-Chao,Bruneau, Christian,Roisnel, Thierry,Gramage-Doria, Rafael

, p. 12893 - 12903 (2019)

Biologically relevant N-arylisoindolinones efficiently underwent arylation reactions under ruthenium catalysis via C-H bond functionalization. The reactions exclusively led to monoarylated products, and only ortho selectivity was observed in the aromatic ring connected to the nitrogen atom. Interestingly, no C-H bond functionalization was observed in the other benzene ring in the ortho position with respect to the carbonyl group. This ruthenium-catalyzed reaction displayed a high functional group tolerance, and it employed readily available and benchmark stable boronic acid and potassium aryltrifluoroborate derivatives as coupling partners. An appealing late-stage functionalization of indoprofen applying this methodology is showcased.

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