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169228-67-5

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169228-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169228-67-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,2,2 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 169228-67:
(8*1)+(7*6)+(6*9)+(5*2)+(4*2)+(3*8)+(2*6)+(1*7)=165
165 % 10 = 5
So 169228-67-5 is a valid CAS Registry Number.

169228-67-5Relevant academic research and scientific papers

Visible-Light Photocatalytic Functionalization of Isocyanides for the Synthesis of Secondary Amides and Ketene Aminals

Cannalire, Rolando,Amato, Jussara,Summa, Vincenzo,Novellino, Ettore,Tron, Gian Cesare,Giustiniano, Mariateresa

, p. 14077 - 14086 (2020/11/20)

A new visible light-induced photocatalytic protocol enabling the formation of secondary amides from electron-poor organic bromides and isocyanides was developed. In addition, the in situ interception of ketenimine intermediates with nitrogen nucleophiles such as amines, hydrazines, and TMSN3 afforded, in a one-pot two-step procedure, valuable scaffolds such as ketene aminals, pyrazolones, and tetrazoles. Mechanistic evidence confirmed a radical pathway where isocyanides acted as radical geminal acceptors generating key imidoyl radical species.

Palladium-catalyzed selective hydrogenolysis of N-alkyl(aryl)-substituted γ-keto amides as an approach to γ-lactams or linear amides

Turova,Berezhnaya,Starodubtseva,Vinogradov

, p. 1065 - 1068 (2016/02/09)

A palladium-catalyzed hydrogenolysis of N-substituted γ-keto amides can proceed with participation of tautomeric 5-hydroxypyrrolidin-2-ones and give either pyrrolidin-2-ones, or linear amides, or their mixtures, depending on the substrate structure.

Preparation of 3-Hydroxyindolin-1-ones and o-Acylbenzamides. A Study of Ring-Chain Tautomerism

Nishio, Takehiko,Yamamoto, Hiroshi

, p. 883 - 892 (2007/10/02)

3-Hydroxyisoindolinones (ring form) as well as their chain tautomers, o-acylbenzamides, were prepared from the reactions of 3-benzalphthalide 1, 3-halophthalides 3, and o-acylbenzoic acids 6 or their esters 7 with amines 2, and those of phthalimides 4 wit

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