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Benzoic acid, 4-fluoro-, propyl ester, also known as 4-fluorobenzoic acid propyl ester, is an organic compound with the chemical formula C10H11FO2. It is a colorless to pale yellow liquid that is soluble in organic solvents and has a molecular weight of 184.19 g/mol. This ester is derived from the parent compound benzoic acid by substituting one hydrogen atom on the benzene ring with a fluorine atom and esterifying the carboxylic acid group with a propyl alcohol. It is used in various applications, including pharmaceuticals, agrochemicals, and as a chemical intermediate in the synthesis of other compounds. Due to its specific functional groups, it may exhibit unique properties compared to its non-fluorinated counterparts, such as altered reactivity or physical characteristics.

2928-10-1

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2928-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2928-10-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,2 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2928-10:
(6*2)+(5*9)+(4*2)+(3*8)+(2*1)+(1*0)=91
91 % 10 = 1
So 2928-10-1 is a valid CAS Registry Number.

2928-10-1Downstream Products

2928-10-1Relevant academic research and scientific papers

Oxidative esterification of alcohols and aldehydes using supported iron oxide nanoparticle catalysts

Rajabi, Fatemeh,Arancon, Rick A.D.,Luque, Rafael

, p. 101 - 103 (2015/02/19)

The synthesis of esters has become an important industrial methodology over the past years because of the role that they serve in the chemical industry. In this study, we present the use of a novel catalyst for the direct conversion of aldehydes into esters. The yields obtained using supported iron oxide nanoparticle catalysts (FeNP) are very high (>90%). The catalyst is also shown to be very stable as shown by the recyclability study (up to 11 times).

p-Fluorobenzoyl Chloride for Characterization of Active Hydrogen Functional Groups by Fluorine-19 Nuclear Magnetic Resonance Spectrometry

Spratt, M. P.,Dorn, H. C.

, p. 2038 - 2043 (2007/10/02)

The base-catalyzed reactions of p-fluorobenzoyl chloride provide a convenient method for (19)F NMR analysis of alcohols, phenols, carboxylic acids, amines, and thiols.The (19)F chemical shift and yield data for p-fluorobenzoyl derivatives for nearly 100 compounds are presented.The yield data for these p-fluorobenzoyl derivatives suggest a simple, and in many cases, quantitative method for introducing a fluorine tagging group.The (19)F chemical shifts indicate a wide chemical shift range (ca. 10 ppm) for a large number of compounds.Furthermore, most chemical classes (e.g., phenols, alcohols, etc.) have fairly well resolved chemical shift regions.

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