852181-17-0 Usage
Description
3-(2-fluoro-4-methylphenyl)propionic acid is a chemical compound with the molecular formula C10H11FO2. It is classified as a non-steroidal anti-inflammatory drug (NSAID) and is commonly used for its anti-inflammatory, analgesic, and antipyretic properties. 3-(2-fluoro-4-methylphenyl)propionic acid is a derivative of propionic acid and contains a fluorine and a methyl group attached to a phenyl ring. It works by inhibiting the production of prostaglandins, which are responsible for inflammation and pain in the body.
Used in Pharmaceutical Industry:
3-(2-fluoro-4-methylphenyl)propionic acid is used as an anti-inflammatory agent for reducing inflammation and pain associated with various conditions such as arthritis, menstrual cramps, and sports injuries. Its analgesic properties make it suitable for the treatment of mild to moderate pain, while its antipyretic effects help in managing fever.
Used in Pain Management:
3-(2-fluoro-4-methylphenyl)propionic acid is used as a pain reliever for managing mild to moderate pain. Its ability to inhibit prostaglandin production helps in reducing pain sensations and providing relief to the affected individuals.
Used in Fever Reduction:
3-(2-fluoro-4-methylphenyl)propionic acid is used as an antipyretic agent for reducing fever. By inhibiting prostaglandin production, it helps in lowering body temperature and providing relief from feverish conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 852181-17-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,1,8 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 852181-17:
(8*8)+(7*5)+(6*2)+(5*1)+(4*8)+(3*1)+(2*1)+(1*7)=160
160 % 10 = 0
So 852181-17-0 is a valid CAS Registry Number.
852181-17-0Relevant articles and documents
Chiral building blocks: Enantioselective syntheses of benzyloxymethyl phenyl propionic acids
Parsons, Jack G.,Stachurska-Buczek, Danuta,Choi, Neil,Griffiths, Peter G.,Huggins, Daniel A.,Krywult, Beata M.,Marino, Sharon T.,Nguyen, Thao,Sheehan, Craig S.,James, Ian W.,Bray, Andrew M.,White, Jonathan M.,Boyce, Rustum S.
, p. 449 - 458 (2007/10/03)
The synthesis of (2S)-2-benzyloxymethyl-3-(2-fluoro-4-methoxyphenyl)- propionic acid, (2S)-2-benzyloxymethyl-3-(2-fluoro-4-methylphenyl)propionic acid and (2S)-2-benzyl-oxymethyl-3-(2,4-dimethylphenyl)propionic acid has been achieved by TiCl4 mediated alkylation of the corresponding (4R)-4-benzyl-3-[3-(2-fluoro-4-methoxyphenyl-, 2-fluoro-4-methylphenyl-, 2,4-dimethylphenyl-)propionyl]-2-oxazolidinones, followed by hydrolysis of the chiral auxiliary. The stereochemistry of the alkylation reaction was confirmed by an X-ray crystal structure of (4R)-4-benzyl-3-[(2S)-2-benzyloxymethyl-3-(2- fluoro-4-methylphenyl)propionyl]-2-oxazolidinone.
