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1-(2,6-dimethoxyphenyl)-2-phenylethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52856-19-6

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52856-19-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52856-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,5 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52856-19:
(7*5)+(6*2)+(5*8)+(4*5)+(3*6)+(2*1)+(1*9)=136
136 % 10 = 6
So 52856-19-6 is a valid CAS Registry Number.

52856-19-6Downstream Products

52856-19-6Relevant academic research and scientific papers

Preparation method of aryl ketone

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Paragraph 0069-0073, (2021/10/11)

The invention discloses a preparation method of aryl ketone. The preparation method comprises the following steps: mixing a phenyl epoxy compound, aryl trifluoromethanesulfonate, a phosphine ligand, a nickel source, alkali and an organic solvent, and conducting reacting in one step under the protection of inert gas to generate aryl ketone. The preparation method disclosed by the invention is simple in process, mild in conditions and low in cost, and paves a way for large-scale industrial production application, such as drug synthesis or natural product synthesis application, of aryl ketone serving as an important organic reaction intermediate.

An improved palladium(II)-catalyzed method for the synthesis of aryl ketones from aryl carboxylic acids and organonitriles

Axelsson, Linda,Veron, Jean-Baptiste,S?vmarker, Jonas,Lindh, Jonas,Odell, Luke R.,Larhed, Mats

supporting information, p. 2376 - 2380 (2014/05/06)

A palladium(II)-catalyzed decarboxylative protocol for the synthesis of aryl ketones has been developed. The addition of TFA was shown to improve the reaction yield and employing THF as solvent enabled the use of solid nitriles and in only a small excess. Using this method, five different benzoic acids reacted with a wide range of nitriles to produce 29 diverse (hetero)aryl ketone derivatives in up to 94% yield.

Synthesis of aryl ketones by palladium(II)-catalyzed decarboxylative addition of benzoic acids to nitriles

Lindh, Jonas,Sjoeberg, Per J. R.,Larhed, Mats

supporting information; experimental part, p. 7733 - 7737 (2011/01/05)

An efficient, sustainable method for the preparation of aryl ketones from ortho-substituted benzoic acids proceeds through their decarboxylation to generate an aryl-palladium species, followed by addition to a nitrile and hydrolysis of the intermediate ketimine.

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