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3-butyl-2-phenyl-2H-azirine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1629159-56-3

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1629159-56-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1629159-56-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,9,1,5 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1629159-56:
(9*1)+(8*6)+(7*2)+(6*9)+(5*1)+(4*5)+(3*9)+(2*5)+(1*6)=193
193 % 10 = 3
So 1629159-56-3 is a valid CAS Registry Number.

1629159-56-3Relevant academic research and scientific papers

-Cycloaddition of 2 H-Azirines with Nitrosoarenes: Visible-Light-Promoted Synthesis of 2,5-Dihydro-1,2,4-oxadiazoles

Cai, Bao-Gui,Chen, Ze-Le,Xu, Guo-Yong,Xuan, Jun,Xiao, Wen-Jing

supporting information, (2019/06/13)

A formal [3 + 2]-cycloaddition reaction of 2H-azirines with nitrosoarenes has been achieved under irradiation by visible light with the assistance of organic dye photoredox catalyst. This method utilizes nitrosoarenes as efficient radical acceptors and pr

Ruthenium-Catalyzed C-C Bond Cleavage of 2H-Azirines: A Formal [3+2+2] Cycloaddition to Fused Azepine Skeletons

Li, Tengfei,Xu, Fen,Li, Xincheng,Wang, Chunxiang,Wan, Boshun

supporting information, p. 2861 - 2865 (2016/02/27)

2H-azirines can serve as three-atom synthons by C-C bond cleavage, however, it involves a high energy barrier under thermal conditions (>50.0 kcal mol-1). Reported is a ruthenium-catalyzed [3+2+2] cycloaddition reaction of 2H-azirines with diyn

Ruthenium-Catalyzed [3 + 2] Cycloaddition of 2H-Azirines with Alkynes: Access to Polysubstituted Pyrroles

Li, Tengfei,Yan, Hao,Li, Xincheng,Wang, Chunxiang,Wan, Boshun

supporting information, p. 12031 - 12037 (2016/12/09)

A ruthenium-catalyzed intermolecular [3 + 2] cycloaddition of 2H-azirines and activated alkynes is reported, which provides polysubstituted pyrroles in moderate to good yields. This approach features a C-N bond cleavage of 2H-azirines by a ruthenium catal

Visible-light-induced formal [3+2] cycloaddition for pyrrole synthesis under metal-free conditions

Xuan, Jun,Xia, Xu-Dong,Zeng, Ting-Ting,Feng, Zhu-Jia,Chen, Jia-Rong,Lu, Liang-Qiu,Xiao, Wen-Jing

supporting information, p. 5653 - 5656 (2014/06/10)

A photocatalytic formal [3+2] cycloaddition of 2H-azirines with alkynes has been achieved under irradiation by visible light in the presence of organic dye photocatalysts. This transformation provides efficient access to highly functionalized pyrroles in good yields and has been applied to the synthesis of drug analogues. A primary trial of photocascade catalysis merging energy transfer and redox neutral reactions was shown to be successful. Photo(chemistry) op: A photocatalytic formal [3+2] cycloaddition of 2H-azirines with alkynes has been established under the irradiation of visible light in the presence of an organic dye. This transformation provides efficient access to highly functionalized pyrroles in good yields and has been applied to the formal synthesis of an inhibitor for HMG-CoA reductase.

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