52962-26-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(1-Acetyl-2-oxopropyl)benzoic acid is used as an analgesic and anti-inflammatory agent for the treatment of various conditions characterized by pain and inflammation, such as arthritis, gout, and menstrual cramps. Its effectiveness in managing these symptoms has led to its widespread prescription by healthcare professionals.
Used in Pain Management:
2-(1-Acetyl-2-oxopropyl)benzoic acid serves as a key component in pain management therapies, providing relief from acute and chronic pain conditions by reducing inflammation and alleviating discomfort.
Used in Inflammation Control:
In conditions where inflammation is a primary concern, such as in certain types of arthritis, 2-(1-Acetyl-2-oxopropyl)benzoic acid is utilized to control inflammation, thereby improving the quality of life for affected individuals.
Available in various forms, including tablets, capsules, and topical gels, 2-(1-Acetyl-2-oxopropyl)benzoic acid offers flexibility in treatment options, allowing healthcare professionals to tailor the administration method to the specific needs of each patient.
Check Digit Verification of cas no
The CAS Registry Mumber 52962-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,9,6 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52962-26:
(7*5)+(6*2)+(5*9)+(4*6)+(3*2)+(2*2)+(1*6)=132
132 % 10 = 2
So 52962-26-2 is a valid CAS Registry Number.
52962-26-2Relevant academic research and scientific papers
Atropisomerism in linear tetrapyrroles
Boiadjiev, Stefan E,Lightner, David A
, p. 7411 - 7421 (2007/10/03)
Novel bilirubin and biliverdin congeners with propionic acids replaced by o-carboxyphenyl exhibit diastereomerism due to axial chirality about the carbon-carbon single bond linking the o-carboxyphenyl group to a pyrrole ring. Evidence for atropisomerism was found even in the monopyrrole precursor, ethyl 3,5-dimethyl-4-(o-carboxyphenyl)pyrrole-2-carboxylate. Like bilirubin, o-carboxyphenyl rubin 1a adopts an intramolecularly hydrogen-bonded ridge-tile conformation in nonpolar solvents. In solutions containing optically active amines or human serum albumin 1a exhibits intense bisignate exciton coupling-type induced circular dichroism for its long wavelength absorption near 400nm.
