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1-Cyclohexene-1-carboxylic acid, 2-[[(4-methylphenyl)sulfonyl]oxy]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

226700-70-5

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226700-70-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226700-70-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,7,0 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 226700-70:
(8*2)+(7*2)+(6*6)+(5*7)+(4*0)+(3*0)+(2*7)+(1*0)=115
115 % 10 = 5
So 226700-70-5 is a valid CAS Registry Number.

226700-70-5Relevant academic research and scientific papers

Pd-Catalyzed Difluoromethylation of Vinyl Bromides, Triflates, Tosylates, and Nonaflates

Chang, Dalu,Gu, Yang,Shen, Qilong

supporting information, p. 6074 - 6078 (2015/04/14)

Pd-catalyzed difluoromethylation of di-, tri- or tetra-substituted vinyl bromides, triflates, tosylates and nonaflates under mild conditions is described. The reaction tolerates a wide range of functional groups, such as bromide, chloride, fluoride, ester, amine, nitrile, and protected carbonyl, thus providing a general route for the preparation of difluoromethylated alkenes. Vinyl fantasy: Pd-catalyzed difluoromethylation of di-, tri-, or tetra-substituted vinyl bromides, triflates, tosylates, and nonaflates under mild conditions is described. The reaction tolerates a wide range of functional groups, such as bromide, chloride, fluoride, ester, amine, nitrile, and protected carbonyl, thus providing a general route for the preparation of difluoromethylated alkenes.

Preparation of α,β-unsaturated esters and amides via external-CO-free palladium-catalyzed carbonylation of alkenyl tosylates

Ueda, Tsuyoshi,Konishi, Hideyuki,Manabe, Kei

supporting information; experimental part, p. 5171 - 5175 (2012/09/25)

Palladium-catalyzed carbonylation of tosylates with phenyl formate is described. This procedure needs neither external carbon monoxide nor any pressure-resistant apparatus. A variety of cyclic and acyclic alkenyl tosylates can be converted into the corresponding phenyl esters in good yields. Furthermore, this method is effective for the one-pot synthesis of α,β-unsaturated amides.

General, robust, and stereocomplementary preparation of β-ketoester enol tosylates as cross-coupling partners utilizing TsCl-N-methylimidazole agents

Nakatsuji, Hidefumi,Ueno, Kanako,Misaki, Tomonori,Tanabe, Yoo

supporting information; body text, p. 2131 - 2134 (2009/05/26)

(Chemical Equation Presented) We have developed a general, robust, and cost-effective method for the (E)- or (Z)-stereocomplementary enol tosylation of β-ketoesters using TsCl-N-methylimidazole (NMI)-Et3N or LiOH. TsCl coupled with NMI formed a

Preparation of enamides via palladium-catalyzed amidation of enol tosylates

Klapars, Artis,Campos, Kevin R.,Chen, Cheng-Yi,Volante, Ralph P.

, p. 1185 - 1188 (2007/10/03)

(Chemical Equation Presented) A Pd-catalyzed coupling of enol tosylates and amides has been developed. Ligand screening revealed dipf as the most general ligand for this transformation. A variety of enol tosylates were coupled to an array of enamides in 5

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