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169295-49-2

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169295-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169295-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,2,9 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 169295-49:
(8*1)+(7*6)+(6*9)+(5*2)+(4*9)+(3*5)+(2*4)+(1*9)=182
182 % 10 = 2
So 169295-49-2 is a valid CAS Registry Number.

169295-49-2Relevant academic research and scientific papers

METHOD FOR PRODUCING ALPHA-ACYLOXYCARBONYL COMPOUND AND NOVEL ALPHA-ACYLOXYCARBONYL COMPOUND

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Page/Page column 7-9, (2013/02/27)

A method for producing an α-acyloxycarbonyl compound of the present invention includes performing an intermolecular reaction between a carboxylic acid and a carbonyl compound selected from the group consisting of ketones, aldehydes, and esters, which have

Redox catalysis of halide ion for formal cross-dehydrogenative coupling: Bromide ion-catalyzed direct oxidative α-acetoxylation of ketones

Nagano, Takashi,Jia, Zhenhua,Li, Xingshu,Yan, Ming,Lu, Gui,Chan, Albert S. C.,Hayashi, Tamio

supporting information; experimental part, p. 929 - 931 (2011/01/09)

A novel catalytic approach for formal cross-dehydrogenative coupling using the redox property of bromide ion is reported. Simple bromide salts MBr can work as catalyst for direct oxidative α-acetoxylation of ketones.

A facile synthesis of secondary α-alkoxy or α-acetoxy aromatic ketones

Lee, Jong Chan,Hong, Taiyoung

, p. 4085 - 4090 (2007/10/03)

The treatment of HNIB with aromatic ketones and subsequent solvolysis using alcohol or acetic acid in one-pot system makes it possible to give corresponding secondary α-alkoxy or α-acetoxy ketones in high yields.

Resolution of Secondary α-Ketoalcohols Catalyzed by Lipase and Inversioon of Stereochemistry

Duh, Tsai-Hui,Wang, Yi-Fong,Wu, Ming-Jung

, p. 579 - 584 (2007/10/02)

Several α-ketoalcohols of synthetic value were resolved using lipase as a catalyst.Lipoprotein lipase (LPL) provided the best rate of hydrolysis and kinetic differentiation.One of these optically pure α-ketoalcohol was converted to (S)-ibuprofen in good optical purity.The stereospecific inversion of (R)-alcohol to (S)-alcohol is described.Key Words Enzymatic resolution; α-Ketoalcohol; (S)-Ibuprofen

Enzymes in Organic Synthesis: Lipase Catalyzed Resolution of Secondary α-Ketoalcohols

Duh, Tsai-Hui,Wang, Yi-Fong,Wu, Ming-Jung

, p. 1793 - 1794 (2007/10/02)

Resolution of several α-ketoalcohols of synthetic value using lipase as a catalyst is described.

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