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294642-63-0

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294642-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 294642-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,4,6,4 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 294642-63:
(8*2)+(7*9)+(6*4)+(5*6)+(4*4)+(3*2)+(2*6)+(1*3)=170
170 % 10 = 0
So 294642-63-0 is a valid CAS Registry Number.

294642-63-0Relevant articles and documents

Access to α-Cyano Carbonyls Bearing a Quaternary Carbon Center by Reductive Cyanation

Ren, Xinyi,Shen, Chaoren,Wang, Guangzhu,Shi, Zhanglin,Tian, Xinxin,Dong, Kaiwu

supporting information, p. 2527 - 2532 (2021/05/05)

Reductive cyanation of tertiary alkyl bromides using electrophilic cyanating reagent and zinc reductant was developed, providing various α-cyano ketones, esters, and carboxamides containing a nitrile-bearing all-carbon quaternary center in good to excellent yields under mild reaction conditions. The corresponding reaction mechanism involving in situ generated organozinc reagent and reactivity distinction was elucidated by density functional theory computation.

Iron-Catalyzed 1,4-Phenyl Migration/Ring Expansion of α-Azido N-Phenyl Amides

Wei, Kaijie,Liang, Siyu,Yang, Tonghao,Yu, Wei

supporting information, p. 8650 - 8654 (2021/11/13)

Herein, we report a novel iron-catalyzed skeleton rearrangement of alkyl azides. Upon treatment with FeCl2 and N-heterocyclic carbene SIPr·HCl in the presence of H2O and Et3N, 2-azido-N,N-diphenylamides underwent 1,4-phenyl migration and ring expansion to give azepin-2-ones in good yield. The reaction proceeds via intramolecular nitrene cycloaddition followed by C-N cleavage, water addition, and electrocyclic ring opening.

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