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4-Fluorobenzoic acid octyl ester is an organic compound with the chemical formula C15H21FO2. It is an ester derivative of 4-fluorobenzoic acid, where the hydroxyl group of the carboxylic acid is replaced by an octyl group. 4-fluorobenzoic acid octyl ester is characterized by its aromatic ring structure with a fluorine atom at the para position, which imparts unique chemical properties. It is a colorless to pale yellow liquid with a mild, fruity odor. 4-Fluorobenzoic acid octyl ester is used in the fragrance industry as a fixative and in the synthesis of other organic compounds. It is also known for its potential applications in pharmaceuticals and agrochemicals due to its ability to influence certain biological processes. The compound is typically synthesized through the esterification of 4-fluorobenzoic acid with octanol, and its properties can be manipulated for specific uses in various industries.

840-77-7

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840-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 840-77-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 840-77:
(5*8)+(4*4)+(3*0)+(2*7)+(1*7)=77
77 % 10 = 7
So 840-77-7 is a valid CAS Registry Number.

840-77-7Downstream Products

840-77-7Relevant academic research and scientific papers

CeO2-catalysed one-pot selective synthesis of esters from nitriles and alcohols

Tamura, Masazumi,Tonomura, Takuya,Shimizu, Ken-Ichi,Satsuma, Atsushi

, p. 984 - 991 (2012)

Thirteen kinds of metal oxides were tested for one-pot selective synthesis of esters from nitriles and alcohols. Ceria (CeO2) showed more than two orders of magnitude higher activity than the other oxides. CeO2 acted as a reusable and effective catalyst for the ester synthesis from various nitriles and alcohols under neutral and solvent-free conditions at 160 °C. This method provides a rare example for the synthesis of heteroaromatic esters, which have been difficult to synthesize by conventional catalytic esterification methods. Valuable esters such as picolinic acid alkyl esters and niacin benzyl esters were synthesized, demonstrating a practical aspect of the present method. Kinetic studies suggested the following reaction mechanism: (1) H2O and ROH dissociate on CeO2, (2) nucleophilic attack of hydroxyl species (OHδ-) to the adsorbed nitrile on CeO2, leading to the formation of the primary amide, (3) nucleophilic attack of alkoxide species (ORδ-) to the amide as the rate-limiting step.

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