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2-(chloromethyl)-N-methyl-N-phenylacrylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1582285-73-1

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1582285-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1582285-73-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,2,2,8 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1582285-73:
(9*1)+(8*5)+(7*8)+(6*2)+(5*2)+(4*8)+(3*5)+(2*7)+(1*3)=191
191 % 10 = 1
So 1582285-73-1 is a valid CAS Registry Number.

1582285-73-1Downstream Products

1582285-73-1Relevant academic research and scientific papers

The photocatalysis synthetic alkaloid (by machine translation)

-

, (2018/11/22)

The present invention provides a catalytic synthesis method of living beings, the alkaloid comprises indole fused ring class and indole spiro compound, the process is as follows: in order to nitrogen aryl acrylamide as raw materials in under the photocatalysis with peroxide synthesis 3 - acetal 2 - indole compound, obtained through hydrolysis 3 - formyl - 2 - indole compound, further reducing synthetic alkaloid, the method routes mild, efficiency is high-efficient. The reaction in the illumination can occur under the room temperature, mild condition, has better substrate versatility and functional group tolerant. (by machine translation)

The carbomethylation of arylacrylamides leading to 3-ethyl-3-substituted indolin-2-one by cascade radical addition/cyclization

Dai, Qiang,Yu, Jintao,Jiang, Yan,Guo, Songjin,Yang, Haitao,Cheng, Jiang

supporting information, p. 3865 - 3867 (2014/04/03)

An FeCl2-promoted carbomethylation of arylacrylamides by di-tert-butyl peroxide (DTBP) is achieved, leading to 3-ethyl-3-substituted indolin-2-one in high yield. The reaction tolerates a series of functional groups, such as cyano, nitro, ethyloxy carbonyl, bromo, chloro, and trifluoromethyl groups. The radical methylation and arylation of the alkenyl group are involved in this reaction. This journal is the Partner Organisations 2014.

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