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(5-fluoro-2-(pyridin-2-yloxy)phenyl)(phenyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1173294-86-4

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1173294-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173294-86-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,2,9 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1173294-86:
(9*1)+(8*1)+(7*7)+(6*3)+(5*2)+(4*9)+(3*4)+(2*8)+(1*6)=164
164 % 10 = 4
So 1173294-86-4 is a valid CAS Registry Number.

1173294-86-4Relevant academic research and scientific papers

Palladium-catalyzed direct ortho aroylation of 2-phenoxypyridines with aldehydes and catalytic mechanism investigation

Chu, Jean-Ho,Chen, Shih-Tien,Chiang, Meng-Fan,Wu, Ming-Jung

, p. 953 - 966 (2015/03/18)

A direct ortho aroylation of 2-phenoxypyridines with aldehydes leading to aryl ketones by the use of palladium(II) acetate, tert-butyl hydroperoxide, and chlorobenzene as the catalyst, oxidant, and solvent, respectively, is presented. Intra- and intermolecular kinetic isotope effects, radical trapping, and controlled experiments were carried out to support the proposed catalytic mechanism for the reaction. Syntheses of (2-hydroxyphenyl)(phenyl)methanones and 1-hydroxy-9H-fluoren-9-ones directed from ortho-aroylated 2-phenoxypyridines were demonstrated.

Pd-catalyzed oxidative acylation of 2-phenoxypyridines with alcohols via C-H bond activation

Kim, Minyoung,Sharma, Satyasheel,Park, Jihye,Kim, Mirim,Choi, Yeonhee,Jeon, Yukyoung,Kwak, Jong Hwan,Kim, In Su

, p. 6552 - 6559 (2013/07/25)

A palladium-catalyzed oxidative acylation of 2-phenoxypyridines with benzylic and aliphatic alcohols via C-H bond activation is described. This protocol represents direct access to biologically active ortho-acylphenol derivatives, and provides new opportunities to use readily available alcohols as starting materials for catalytic acylation reactions.

Palladium-catalyzed decarboxylative coupling of α-oxocarboxylic acids with C(sp2)-H of 2-aryloxypyridines

Yao, Jinzhong,Feng, Ruokun,Wu, Zaihong,Liu, Zhanxiang,Zhang, Yuhong

, p. 1517 - 1522 (2013/06/27)

An efficient palladium-catalyzed decarboxylative ortho-acylation of 2-aryloxypyridines with α-oxocarboxylic acids is described. In this new transformation, the aromatic C(sp2)-H bond was successfully acylated to give diverse aromatic ketones regioselectively in moderate to good yields. The pyridine group can be removed easily after the acylation to give the corresponding 2-hydroxy aromatic ketones. Copyright

Palladium-catalyzed acylation of sp2 C-H bond: Direct access to ketones from aldehydes

Jia, Xiaofei,Zhang, Shouhui,Wang, Wenhui,Luo, Fang,Cheng, Jiang

supporting information; experimental part, p. 3120 - 3123 (2009/12/06)

A palladium-catalyzed direct access to ketones from aldehydes via C-H cleavage of arenes is described. The procedure utilizes air as a clean and free terminal oxidant.

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