51671-72-8 Usage
Classification
Nonsteroidal anti-inflammatory drug (NSAID)
A drug class used to relieve pain and reduce inflammation
Common uses
Arthritis, menstrual discomfort
Chemical structure
Benzoic acid molecule with a carbonyl group attached to a 4-hydroxy-3-methylphenyl group
The specific arrangement of atoms and functional groups in the molecule
Mechanism of action
Inhibition of prostaglandin production
Prostaglandins are molecules involved in the inflammatory response
Administration
Oral medication, topical gel
The ways in which the drug can be taken
Enzyme blocking
Reduces pain and inflammation
By blocking enzymes responsible for producing prostaglandins
Side effects
Gastrointestinal irritation, increased risk of cardiovascular events
Potential negative effects of using the drug
Precautions
Use with caution, under the supervision of a healthcare professional
To minimize potential side effects and ensure safe usage
Check Digit Verification of cas no
The CAS Registry Mumber 51671-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,7 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51671-72:
(7*5)+(6*1)+(5*6)+(4*7)+(3*1)+(2*7)+(1*2)=118
118 % 10 = 8
So 51671-72-8 is a valid CAS Registry Number.
51671-72-8Relevant articles and documents
-
Ziegler,Zigeuner
, (1949)
-
3,3-Diarylphthalides. Part I. Friedlaender reaction of 3′-alkylphenolphthaleins
Ruminski
, p. 908 - 914 (2007/10/03)
Friedlaender reaction was investigated, starting from 3′-alkyl-derivatives of phenolphthalein 1-3 (alkyl = Me, Et and i-Pr) and hydroxylamine in strongly alkaline medium. The process was found to give, after acidic hydrolysis of primarily formed anil-type semi-products, a mixture of two 2-aroylbenzoic acids (2-ABAs) in each case. Identification and quantification of 2-ABAs were carried out within RP-HPLC on ODS column. Based on quantitative results, migratory aptitude (MA) parameter values of ionized 4-hydroxy-3-alkylphenyl nuclei were calculated, taking an unsubstituted ionized 4-hydroxyphenyl ring as a standard.
