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α-Ethoxy-p-methylacetophenone, also known as ethyl 4-acetyl-3-methoxybenzoate, is an organic compound with the chemical formula C11H12O3. It is a colorless to pale yellow liquid with a molecular weight of 192.21 g/mol. α-ethoxy-p-methylacetophenone is characterized by the presence of an acetophenone moiety, with a methyl group at the para position and an ethoxy group at the alpha position. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. α-Ethoxy-p-methylacetophenone is typically synthesized through the Friedel-Crafts acylation of anisole with acetyl chloride in the presence of a Lewis acid catalyst, such as aluminum chloride. The compound is sensitive to light and heat, and it is recommended to store it in a cool, dry place, away from direct sunlight.

14869-40-0

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14869-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14869-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,6 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14869-40:
(7*1)+(6*4)+(5*8)+(4*6)+(3*9)+(2*4)+(1*0)=130
130 % 10 = 0
So 14869-40-0 is a valid CAS Registry Number.

14869-40-0Downstream Products

14869-40-0Relevant articles and documents

Direct Synthesis of α-Alkoxy Ketones by Oxidative C–O Bond Formation

Yu, Hui,Xu, Yilan,Fang, Yan,Dong, Rui

, p. 5257 - 5262 (2016)

A convenient method to prepare α-alkoxy ketones has been developed by oxidative coupling of aryl methyl ketones and alcohols. With aqueous tert-butyl hydroperoxide (6.0 equiv.) as the oxidant, tetrabutylammonium iodide (20 mol-%) as the catalyst, and TsNHNH2(1.0 equiv.) as the additive, ketones underwent direct alkoxylation to give α-methoxy or α-ethoxy ketones in moderate to good yields.

ACID-CATALYZED DECOMPOSITION OF DIAZO CARBONYL COMPOUNDS. II. SYNTHESIS OF 2- OR 5-HETEROATOM-SUBSTITUTED OXAZOLES.

Ibata,Yamashita,Kashiuchi,Nakano,Nakawa

, p. 2450 - 2455 (2007/10/02)

The BF//3-catalyzed decomposition of m- and p-substituted alpha -diazoacetophenones in excess of methyl thiocyanate and ethyl thiocyanate gave the corresponding 2-methylthio-, and 2-ethylthio-5-aryloxazoles, respectively in good yields along with s-alkyl-

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