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(E)-2-(3-(perfluorophenyl)prop-1-en-1-yl)naphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1609490-06-3

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1609490-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609490-06-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,4,9 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1609490-06:
(9*1)+(8*6)+(7*0)+(6*9)+(5*4)+(4*9)+(3*0)+(2*0)+(1*6)=173
173 % 10 = 3
So 1609490-06-3 is a valid CAS Registry Number.

1609490-06-3Downstream Products

1609490-06-3Relevant academic research and scientific papers

Palladium-Catalyzed Direct C-H Allylation of Electron-Deficient Polyfluoroarenes with Alkynes

Zheng, Jun,Breit, Bernhard

supporting information, p. 1866 - 1870 (2018/04/16)

A palladium-catalyzed intermolecular direct C-H allylation of polyfluoroarenes with alkynes is reported. Unlike classic hydroarylation reactions, alkynes are used as allylic electrophile surrogates in this direct aromatic C-H allylation. As an atom-economic and efficient method, various linear allylated fluoroarenes were synthesized from two simple and easy-to-access feedstocks in good to excellent yields, as well as regio- and stereoselectivity.

Palladium-catalyzed aerobic oxidative allylic C-H arylation of alkenes with polyfluorobenzenes

Jiang, Huanfeng,Yang, Wanfei,Chen, Huoji,Li, Jianxiao,Wu, Wanqing

, p. 7202 - 7204 (2014/07/07)

An aerobic oxidative cross-coupling reaction of alkenes with polyfluorobenzenes, through palladium-catalyzed allylic C-H activation, is reported. This attractive route provides a new way to forge allylic C-C bonds of valuable products, in good yields, with high regioselectivity.

Regio- and stereoselective allylic C-H arylation with electron-deficient arenes by 1,1′-Bi-2-naphthol-palladium cooperation

Wang, Gang-Wei,Zhou, An-Xi,Li, Shi-Xia,Yang, Shang-Dong

supporting information, p. 3118 - 3121 (2014/06/23)

A palladium-catalyzed allylic C-H arylation reaction with electron-deficient arenes with high regio- and stereoselectivity is reported. This work represents the first successful use of 1,1′-bi-2-naphthol as the ancillary ligand in allylic C-H activation, which is the key factor for chemoselectivity. Furthermore, high selectivity allylic C-H acetoxylation and amination were also successfully achieved under the same catalytic system.

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