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Acetamide, N-(4-phenyl-2-butenyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

229156-95-0

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229156-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 229156-95-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,9,1,5 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 229156-95:
(8*2)+(7*2)+(6*9)+(5*1)+(4*5)+(3*6)+(2*9)+(1*5)=150
150 % 10 = 0
So 229156-95-0 is a valid CAS Registry Number.

229156-95-0Downstream Products

229156-95-0Relevant academic research and scientific papers

Photocatalyzed Amidoarylation of 1,3-Butadiene

Gosset, Cyrille,Moncomble, Aurélien,Dumont, Clément,Pellegrini, Sylvain,Bousquet, Till,Sauthier, Mathieu,Pélinski, Lydie

, p. 3100 - 3104 (2020)

1,3-Butadiene is involved in a photocatalyzed amidoarylation reaction that allows the synthesis of N-allyl amides. The reaction was evaluated on a wide range of aryl diazonium salts and nitriles as co-reactants. Selectivity issues were studied from the help of a computational approach. (Figure presented.).

Ir-Catalyzed Intermolecular Branch-Selective Allylic C-H Amidation of Unactivated Terminal Olefins

Lei, Honghui,Rovis, Tomislav

supporting information, p. 2268 - 2273 (2019/03/05)

An efficient method for intermolecular branch-selective allylic C-H amidation has been accomplished via Ir(III) catalysis. The reaction proceeds through initial allylic C-H activation, supported by the isolation and crystallographic characterization of an allyl-Ir(III) intermediate, followed by a subsequent oxidative amidation with readily available dioxazolones as nitrenoid precursors. A diverse range of amides are successfully installed at the branched position of terminal alkenes in good yields and regioselectivities. Importantly, the reaction allows the use of amide-derived nitrenoid precursors avoiding problematic Curtius-type rearrangements.

New results on the functionalization of terminal alkenes by cross- metathesis reactions

Blanco, Olga M.,Castedo, Luis

, p. 557 - 558 (2007/10/03)

The ruthenium-catalyzed reaction of allylbenzene with several types of alkene provides good yields of the cross-metathesis products regardless of the structural characteristics of the alkene.

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