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methyl 2-{[(4-methylphenyl)sulfonyl](2-propen-1-yl)amino}benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

928708-41-2

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928708-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 928708-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,7,0 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 928708-41:
(8*9)+(7*2)+(6*8)+(5*7)+(4*0)+(3*8)+(2*4)+(1*1)=202
202 % 10 = 2
So 928708-41-2 is a valid CAS Registry Number.

928708-41-2Relevant academic research and scientific papers

Cobalt-catalyzed cyclization with the introduction of cyano, acyl and aminoalkyl groups

Hori, Hiroto,Arai, Shigeru,Nishida, Atsushi

supporting information, p. 4783 - 4788 (2019/05/24)

An efficient synthesis of carbo-and heterocycles using CC, CO and CN bonds under cobalt catalysis is described. The substituents on olefins are key for controlling the regio-and chemoselectivity in the initial hydrogen atom transfer step and quaternary carbons are efficiently constructed under mild conditions. Cyclopropane cleavage and tandem cyclization give highly functionalized bicyclic skeletons in a single operation.

Oxidative cyclization of alkenoic acids promoted by AgOAc

Carrillo-Arcos, Ulises A.,Rojas-Ocampo, Jonathan,Porcel, Susana

, p. 479 - 483 (2016/01/09)

Alkenoic acids derived from salicylic acid and analogues undergo an unexpected oxidative cyclization process triggered by AgOAc leading to 4H-benzo[d][1,3]dioxin-4-ones. The process is affected by the substitution on the aryl and the allyl units.

Regioselective silver-mediated Kondakov-Darzens olefin acylation

Barczak, Nicholas T.,Jarvo, Elizabeth R.

supporting information; experimental part, p. 12912 - 12916 (2011/12/04)

Enone construction: A silver-mediated olefin acylation reaction is described, in which five-, six-, and -seven-membered rings, tetrasubstituted olefins, bridged bicycles, spirocycles, and benzoxepinones are prepared. Highly selective intermolecular reactions are coupled to a Nazarov cyclization for the effective preparation of cyclopentenones, including the core of modhephene (see scheme). Copyright

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