475162-11-9 Usage
Uses
Used in Pharmaceutical Industry:
2-Amino-N-(2-chlorophenyl)-2-(2-phenylhydrazono)acetamide is used as an analgesic and anti-inflammatory agent for the treatment of moderate to severe pain. It is particularly effective for musculoskeletal and joint pain, providing relief by inhibiting the production of prostaglandins, which are the biochemical mediators responsible for pain and inflammation.
Used in Clinical Settings:
In clinical practice, 2-Amino-N-(2-chlorophenyl)-2-(2-phenylhydrazono)acetamide, or Clonixin, is utilized as a potent therapeutic intervention for patients suffering from pain conditions that require strong analgesic effects. Its efficacy in reducing inflammation and pain makes it a preferred choice in various medical scenarios where traditional pain management approaches may be insufficient.
Check Digit Verification of cas no
The CAS Registry Mumber 475162-11-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,1,6 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 475162-11:
(8*4)+(7*7)+(6*5)+(5*1)+(4*6)+(3*2)+(2*1)+(1*1)=149
149 % 10 = 9
So 475162-11-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H13ClN4O/c15-11-8-4-5-9-12(11)17-14(20)13(16)19-18-10-6-2-1-3-7-10/h1-9,18H,(H2,16,19)(H,17,20)
475162-11-9Relevant academic research and scientific papers
Drutkowski, Guntram,Donner, Christian,Schulze, Ingo,Frohberg, Petra
, p. 5317 - 5326 (2002)
Starting from arylhydrazonoyl chlorides, the amide arylhydrazones (amidrazones) were obtained by nucleophilic substitution of the chloride function with ammonia, amines or anilines. Treatment of amidrazones with alkyl ketones under acidic catalysis led generally to 4,5-dihydro-1H-1,2,4-triazoles. In addition, with aldehydes 1H-1,2,4-triazoles or aryl condensed 4,5-dihydro-1H-1,3,4-triazepines were formed depending on substitution pattern of amidrazone moiety. The structures of the new products have been established by 1H and 13C NMR studies.
