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2-(ethylamino)-5-fluorobenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1315366-67-6

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1315366-67-6 Usage

Benzoic acid family

2-(ethylamino)-5-fluorobenzoic acid belongs to the benzoic acid family, which is a group of organic compounds that have a benzene ring with a carboxyl group attached to it.

Fluorine substituent at the 5 position

The presence of a fluorine atom attached to the 5th carbon of the benzene ring is a key feature of 2-(ethylamino)-5-fluorobenzoic acid.

Ethylamino group at the 2 position

The presence of an ethylamino group (an amino group attached to an ethyl group) attached to the 2nd carbon of the benzene ring is another key feature of 2-(ethylamino)-5-fluorobenzoic acid.

Derivative of salicylic acid

2-(ethylamino)-5-fluorobenzoic acid is a modified version of salicylic acid, which is a naturally occurring organic compound that has similar chemical properties.

Building block for pharmaceuticals and agrochemicals

2-(ethylamino)-5-fluorobenzoic acid is commonly used in organic synthesis to make other compounds that are used in the production of pharmaceuticals and agrochemicals.

Potential intermediate for other fluorinated organic compounds

2-(ethylamino)-5-fluorobenzoic acid can be used as an intermediate in the production of other fluorinated organic compounds.

Biological activities

2-(ethylamino)-5-fluorobenzoic acid has been studied for its potential biological activities, including its ability to reduce inflammation and relieve pain.

Check Digit Verification of cas no

The CAS Registry Mumber 1315366-67-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,3,6 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1315366-67:
(9*1)+(8*3)+(7*1)+(6*5)+(5*3)+(4*6)+(3*6)+(2*6)+(1*7)=146
146 % 10 = 6
So 1315366-67-6 is a valid CAS Registry Number.

1315366-67-6Downstream Products

1315366-67-6Relevant academic research and scientific papers

Synthesis of 1-substituted 4(1H)-quinazolinones under solvent-free conditions

Wang, Yao,Zhang, Mei,Cao, Shengli,Lin, Huihui,Gao, Man,Li, Zhongfeng

experimental part, p. 2715 - 2727 (2012/07/14)

(Chemical Equation Presented) Heating a mixture of 2-(N-alkylamino)benzoic acids, triethyl orthoformate, and ammonium acetate under solvent-free conditions generated 1-substituted 4(1H)- quinazolinones in 73-99% yields. Moreover, a possible reaction pathway was proposed. Copyright Taylor & Francis Group, LLC.

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