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(Z)-ethyl 4-bromo-2,2-difluoro-4-phenylbut-3-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1628218-63-2

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1628218-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1628218-63-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,8,2,1 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1628218-63:
(9*1)+(8*6)+(7*2)+(6*8)+(5*2)+(4*1)+(3*8)+(2*6)+(1*3)=172
172 % 10 = 2
So 1628218-63-2 is a valid CAS Registry Number.

1628218-63-2Downstream Products

1628218-63-2Relevant academic research and scientific papers

Copper-catalyzed fluoroalkylation of alkynes, and alkynyl & vinyl carboxylic acids with fluoroalkyl halides

Ma, Jing-Jing,Yi, Wen-Bin

, p. 4295 - 4299 (2017)

Copper-catalyzed fluoroalkylation of alkynes and alkynyl carboxylic acids has been achieved with high functional-group tolerance and excellent regio- and stereoselectivities. A variety of fluoroalkyl halides including ethyl bromodifluoroacetate can be employed. Additionally, an unprecedented decarboxylative fluoroalkylation of α, β-unsaturated carboxylic acids has been achieved via a radical pathway.

Copper-mediated direct functionalization of unsaturated C-C bonds with ethyl bromo(difluoro)acetate: A straightforward access to highly valuable difluoromethylated alkenes

Belhomme, Marie-Charlotte,Dru, Delphine,Xiong, Heng-Ying,Cahard, Dominique,Besset, Tatiana,Poisson, Thomas,Pannecoucke, Xavier

supporting information, p. 1859 - 1870 (2014/07/22)

A copper-mediated fluorofunctionalization of alkenes and alkynes has been developed. This method provides ready access to trisubstituted difluoromethylated olefins (from dihydropyrans, glycal derivatives, or terminal alkynes) or to tetrasubstituted olefins (from disubstituted alkynes). The products were obtained in good to high yields with acceptable E/Z selectivities. Finally, a first direct route to difluoromethylated alkynes is reported, albeit with low yields. Georg Thieme Verlag Stuttgart New York.

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