80854-22-4 Usage
Explanation
This is the chemical name of the compound, which is also known as fenoprofen.
Explanation
Fenoprofen belongs to a class of drugs called NSAIDs, which are commonly used to alleviate pain and reduce inflammation.
Explanation
Fenoprofen works by inhibiting the production of certain substances in the body that cause pain and inflammation, such as prostaglandins.
Explanation
This chemical is frequently used to treat various conditions related to joint and muscle pain, inflammation, and stiffness.
Explanation
Although fenoprofen is effective in alleviating pain and reducing inflammation, it may also cause some side effects that can affect the stomach, blood, and kidneys.
Classification
Nonsteroidal anti-inflammatory drug (NSAID)
Function
Inhibits production of pain-causing substances
Common uses
Treatment of rheumatoid arthritis, osteoarthritis, and musculoskeletal disorders
Side effects
Potential stomach ulcers, bleeding, and kidney problems
Check Digit Verification of cas no
The CAS Registry Mumber 80854-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,5 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80854-22:
(7*8)+(6*0)+(5*8)+(4*5)+(3*4)+(2*2)+(1*2)=134
134 % 10 = 4
So 80854-22-4 is a valid CAS Registry Number.
80854-22-4Relevant articles and documents
Palladium-Catalyzed Distal m-C-H Functionalization of Arylacetic Acid Derivatives
Srinivas, Dasari,Satyanarayana, Gedu
supporting information, p. 7353 - 7358 (2021/10/01)
Herein, we present m-C-H olefination on derivatives of phenylacetic acids by tethering with a simple nitrile-based template through palladium catalysis. Notably, the versatility of the method is evaluated with a wide range of phenylacetic acid derivatives for obtaining the meta-olefination products in fair to excellent yields with outstanding selectivities under mild conditions. Significantly, the present strategy is successfully exemplified for the synthesis of drugs/natural product analogues (naproxen, ibuprofen, paracetamol, and cholesterol).
NAPHTHALENONE COMPOUNDS EXHIBITING PROLYL HYDROXYLASE INHIBITORY ACTIVITY, COMPOSITIONS, AND USES THEREOF
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Page/Page column 175, (2008/12/06)
Compounds of Formula (I) and Formula (II) are useful as inhibitors of HIF prolyl hydroxylases. Compounds of Formula(I) and Formula (II) have the following structures, where the definitions of the variables are provided herein.
