25173-75-5 Usage
General Description
3-(2,5-DIMETHYLPHENYL)PROPIONIC ACID is an organic compound with the chemical formula C11H14O2. It is a derivative of propionic acid and contains a dimethylphenyl group attached to the third carbon of the propionic acid chain. This chemical is commonly used as a nonsteroidal anti-inflammatory drug (NSAID) due to its ability to reduce inflammation and pain. It works by inhibiting the production of prostaglandins, which are responsible for causing pain and inflammation in the body. 3-(2,5-DIMETHYLPHENYL)PROPIONIC ACID is often administered orally in the form of tablets or capsules and is prescribed for the treatment of various conditions such as arthritis, menstrual cramps, and minor injuries. However, it may have potential side effects such as stomach irritation, gastrointestinal bleeding, and kidney problems, so it should be used with caution and under the supervision of a healthcare professional.
Check Digit Verification of cas no
The CAS Registry Mumber 25173-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,7 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25173-75:
(7*2)+(6*5)+(5*1)+(4*7)+(3*3)+(2*7)+(1*5)=105
105 % 10 = 5
So 25173-75-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O2/c1-8-3-4-9(2)10(7-8)5-6-11(12)13/h3-4,7H,5-6H2,1-2H3,(H,12,13)
25173-75-5Relevant articles and documents
Iron-catalyzed, highly regioselective synthesis of α-aryl carboxylic acids from styrene derivatives and CO2
Greenhalgh, Mark D.,Thomas, Stephen P.
, p. 11900 - 11903 (2012/09/07)
The iron-catalyzed hydrocarboxylation of aryl alkenes has been developed using a highly active bench-stable iron(II) precatalyst to give α-aryl carboxylic acids in excellent yields and with near-perfect regioselectivity. Using just 1 mol % FeCl2, bis(imino)pyridine 6 (1 mol %), CO 2 (atmospheric pressure), and a hydride source (EtMgBr, 1.2 equiv), a range of sterically and electronically differentiated aryl alkenes were transformed to the corresponding α-aryl carboxylic acids (up to 96% isolated yield). The catalyst was found to be equally active with a loading of 0.1 mol %. Preliminary mechanistic investigations show that an iron-catalyzed hydrometalation is followed by transmetalation and reaction with the electrophile (CO2).
