| Identification | More |  [Name]
  Clonixin |  [CAS]
  17737-65-4 |  [Synonyms]
  2-[(3-chloro-2-methylphenyl)amino]-3-pyridinecarboxylic acid CLONIXIC ACID CLONIXIN 3-Pyridinecarboxylic acid, 2-[(3-chloro-2-methylphenyl)amino]- CLONIXIC ACID (CLONIXIN) 2-(3-CHLORO-2-METHYLPHENYLAMINO)NICOTINIC ACID 2-(3-Chloro-2-methylanilino)pyridine-3-carboxylic acid 2-(3-Chloro-o-toluidino)nicotinic acid Sch-10304 |  [EINECS(EC#)]
  241-730-1 |  [Molecular Formula]
  C13H11ClN2O2 |  [MDL Number]
  MFCD00864292 |  [Molecular Weight]
  262.69 |  [MOL File]
  17737-65-4.mol |  
 | Chemical Properties | Back Directory |  [Melting point ]
  233-235° |  [Boiling point ]
  410.2±45.0 °C(Predicted) |  [density ]
  1.3230 (rough estimate) |  [refractive index ]
  1.5270 (estimate) |  [storage temp. ]
  Keep in dark place,Inert atmosphere,Room temperature |  [solubility ]
  DMSO: soluble15mg/mL, clear |  [form ]
  powder |  [pka]
  1.69±0.36(Predicted) |  [color ]
  white to beige |  [Merck ]
  14,2392 |  [CAS DataBase Reference]
  17737-65-4(CAS DataBase Reference) |  
 | Safety Data | Back Directory |  [Hazard Codes ]
  Xn |  [Risk Statements ]
  20/21/22 |  [Safety Statements ]
  36/37 |  [WGK Germany ]
  3 |  [RTECS ]
  QT0960000 |  [HS Code ]
  2933.39.9200 |  [Toxicity]
  LD50 in male mice, rats (mg/kg):  415, 335 orally; 198, 148 i.p.; 296, 325 s.c. (Tanaka) |  
 | Hazard Information | Back Directory |  [Uses]
  Analgesic. |  [Uses]
  Clonixin is a non-steroidal anti-inflammatory drug. It also has analgesic, antipyretic, and platelet-inhibitory actions. The compound has been reported to block prostaglandin synthesis, and to block inward calcium currents. |  [Definition]
  ChEBI: A pyridinemonocarboxylic acid that is nicotinic acid substituted at position 2 by a (2-methyl-3-chlorophenyl)amino group. Used (as its lysine salt) for treatment of renal colic, muscular pain and moderately severe migraine attacks. |  [Biological Activity]
  Clonixin is a non steroidal anti inflammatory drug (NSAID) with analgesic properties. The compound has been reported to block prostaglandin synthesisand to block inward calcium currents. |  
  
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