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Benzoic acid, 4-methoxy-, 4-fluorophenyl ester, also known as 4-methoxybenzoic acid 4-fluorophenyl ester, is a chemical compound with the molecular formula C14H11FO3. It is an ester derivative of benzoic acid, where the hydroxyl group of the carboxylic acid is replaced by a 4-fluorophenyl group, and a methoxy group is attached to the benzene ring at the 4-position. Benzoic acid, 4-methoxy-, 4-fluorophenyl ester is characterized by its aromatic structure and exhibits properties typical of esters, such as a sweet, fruity odor. It is used in various applications, including the synthesis of pharmaceuticals and as a chemical intermediate in the production of certain specialty chemicals. The compound's specific structure and functional groups make it a valuable component in organic chemistry and industrial processes.

729-39-5

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729-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 729-39-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 729-39:
(5*7)+(4*2)+(3*9)+(2*3)+(1*9)=85
85 % 10 = 5
So 729-39-5 is a valid CAS Registry Number.

729-39-5Relevant academic research and scientific papers

Decarboxylative Hydroxylation of Benzoic Acids

Ritter, Tobias,Su, Wanqi,Xu, Peng

supporting information, p. 24012 - 24017 (2021/10/06)

Herein, we report the first decarboxylative hydroxylation to synthesize phenols from benzoic acids at 35 °C via photoinduced ligand-to-metal charge transfer (LMCT)-enabled radical decarboxylative carbometalation. The aromatic decarboxylative hydroxylation is synthetically promising due to its mild conditions, broad substrate scope, and late-stage applications.

Transition-Metal-Free DMAP-Mediated Aromatic Esterification of Amides with Organoboronic Acids

Guo, Jiarui,Liu, Lantao,Wang, Tao,Wang, Yanqing,Xu, Kai,Zhang, Yuheng

supporting information, p. 3274 - 3277 (2021/06/26)

A new, transition-metal-free, effective method for aromatic esterification of amides with organoboronic acids has been developed. A wide range of benzoate derivatives were obtained with yields ranging from moderate to good. The catalytic reaction shows a broad substrate scope and excellent functional group tolerance. Conceptually, DMAP mediates the reaction and is crucial for this transformation.

N-heterocyclic carbene-catalyzed aerobic oxidative direct esterification of aldehydes with organoboronic acids

Meng, Jing-Jing,Gao, Min,Wei, Yu-Ping,Zhang, Wen-Qin

experimental part, p. 872 - 875 (2012/07/03)

A simple procedure affording benzoates through a NHC-catalyzed aerobic oxidative esterification of aldehydes with organoboronic acids has been disclosed. This process allows access to a wide variety of aromatic esters in good to excellent yields under simple, efficient, and sustainable reaction conditions (see scheme).

Palladium-catalyzed aromatic esterification of aldehydes with organoboronic acids and molecular oxygen

Qin, Changming,Wu, Huayue,Chen, Jiuxi,Liu, Miaochang,Cheng, Jiang,Su, Weike,Ding, Jinchang

supporting information; experimental part, p. 1537 - 1540 (2009/04/07)

A palladium-catalyzed aromatic esterification reaction of aldehydes with arylboronic acids under an air atmosphere was achieved. This reaction tolerates many functional groups and provides aryl benzoate derivatives with yields ranging from moderate to good. Dioxygen takes part in the reaction and is crucial for this transformation.

NOVEL BENZOTHIAZEPINE AND BENZOTHIEPINE COMPOUNDS

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Example P424, (2010/11/24)

A pharmaceutical useful as a therapeutic agent and a preventive agent for hyperlipemia, and a pharmaceutical useful as a therapeutic agent and a preventive agent for hepatic disorders associated with cholestasis, particularly, primary biliary cirrhosis an

The synthesis of 4-(4-[11C]methoxyphenyl)-5-fluoro-2-hydroxyphenyl)-methylene-aminobutyric acid, as a potential radioligand for the GABA receptor in the brain

De Vos,Slegers

, p. 643 - 652 (2007/10/02)

A procedure for the synthesis of 4-(4-[11C]methoxyphenyl)-(5fluoro-2-hydroxyphenyl)-methylene-aminobutyric acid has been developed. The production entailed a O-methylation of 5-fluoro-2-hydroxy-4'-hydroxybenzophenone with cyclotron produced [s

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