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N-2-butenyl-N-(phenylmethyl)-2-propenoylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

160925-27-9

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160925-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160925-27-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,9,2 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 160925-27:
(8*1)+(7*6)+(6*0)+(5*9)+(4*2)+(3*5)+(2*2)+(1*7)=129
129 % 10 = 9
So 160925-27-9 is a valid CAS Registry Number.

160925-27-9Downstream Products

160925-27-9Relevant academic research and scientific papers

Indium as a radical initiator in aqueous media: Intermolecular alkyl radical addition to C=N and C=C bond

Miyabe, Hideto,Ueda, Masafumi,Nishimura, Azusa,Naito, Takeaki

, p. 4227 - 4235 (2007/10/03)

The carbon-carbon bond-forming method in aqueous media was investigated by using indium as a single-electron transfer radical initiator. The indium-mediated intermolecular alkyl radical addition to imine derivatives and electron-deficient C=C bond proceeded effectively.

Radical Cyclisation in Heterocycle Synthesis. Part 1. Sulfanyl Radical Addition-Cyclisation of Dienylamides for Lactam Synthesis

Naito, Takeaki,Honda, Yuko,Miyata, Okiko,Ninomiya, Ichiya

, p. 19 - 26 (2007/10/02)

A new method for the synthesis of five- to eight-membered lactams by sulfanyl radical mediated-cyclisation of dienylamides is described.The sulfanyl radical addition-cyclisation of the dienylamide 1 was systematically investigated under four different conditions and was found to give the cyclised lactams 2-6 in 54-79percent yield.The stereo- and regio-selectivity of sulfanyl radical addition-cyclisation was established from the preferential formation of the trans-cyclised lactam 3 and also from the substituent effects in the cyclisation of the dienylamides 11-18.The sulfanyl radical mediated addition-cyclisation was successfully applied to the construction of the six- and eight-membered lactams 28a, b.

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