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2-(2-Fluorobenzoyl)benzoic acid is a synthetic organic compound characterized by its molecular formula C14H9FO3. 2-(2-fluorobenzoyl)benzoic acid features a benzoic acid core, with a fluorobenzoyl group attached at the 2-position. The presence of the fluorine atom in the 2-position of the benzoyl group introduces a unique electronic and steric effect, which can significantly alter the chemical properties and reactivity of the molecule compared to its non-fluorinated analogs. 2-(2-fluorobenzoyl)benzoic acid is of interest in various fields, including pharmaceuticals and materials science, due to its potential applications in the development of new drugs and advanced materials. Its synthesis and properties are subjects of ongoing research, with the aim of understanding its behavior in different chemical environments and its potential use in the creation of new compounds with specific therapeutic or functional properties.

7613-47-0

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7613-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7613-47-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,1 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7613-47:
(6*7)+(5*6)+(4*1)+(3*3)+(2*4)+(1*7)=100
100 % 10 = 0
So 7613-47-0 is a valid CAS Registry Number.

7613-47-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-fluorobenzoyl)benzoic acid

1.2 Other means of identification

Product number -
Other names 2-(2-Fluor-benzoyl)-benzoesaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:7613-47-0 SDS

7613-47-0Relevant academic research and scientific papers

Palladium-catalyzed chemoselective decarboxylative ortho acylation of benzoic acids with α-oxocarboxylic acids

Miao, Jinmin,Ge, Haibo

supporting information, p. 2930 - 2933 (2013/07/26)

Palladium-catalyzed chemoselective decarboxylative cross coupling of benzoic acids with α-oxocarboxylic acids was realized via an arene sp 2 C-H functionalization process. This work represents the first example of transition-metal-catalyzed cro

Decarboxylative C-H arylation of benzoic acids under radical conditions

Seo, Sangwon,Slater, Mark,Greaney, Michael F.

supporting information; scheme or table, p. 2650 - 2653 (2012/07/27)

A decarboxylative radical cyclization reaction has been developed for the synthesis of fluorenones. The reaction uses Ag(I)/K2S 2O8 to oxidatively decarboxylate an aroylbenzoic acid to an aryl radical, which undergoes cyclization to afford fluorenone products in good yield.

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