CAS 15307-93-4
:2,6-Dicloro-N-fenilbenzenamina
- 2,6-Dichloro Diphenylamine
- 2,6-Dichloro-N-phenylbenzenamine
- 2,6-dichloro-N-phenylaniline
- Benzenamine, 2,6-dichloro-N-phenyl-
- Decarboxymethyl diclofenac
- Diphenylamine, 2,6-dichloro-
- N-(2,6-Dichlorophenyl)-N-phenylamine
- N-(2,6-Dichlorophenyl)aniline
- N-Phenyl-2,6-dichloroaniline
- 2,6-Dichlorodiphenylamine
2,6-Dichlorodiphenylamine
CAS:Fórmula:C12H9Cl2NPureza:>98.0%(GC)Cor e Forma:White to Amber to Dark green powder to crystalPeso molecular:238.11Diclofenac Impurity 1 (2,6-Dichlorodiphenylamine)
CAS:Fórmula:C12H9Cl2NCor e Forma:Pale Yellow SolidPeso molecular:238.112,6-Dichlorodiphenylamine
CAS:Produto ControladoFórmula:C12H9Cl2NCor e Forma:NeatPeso molecular:238.11N-(2,6-Dichlorophenyl)aniline
CAS:Produto ControladoApplications N-(2,6-Dichlorophenyl)aniline is an analog of Diclofenac (D436450), a nonsteroidal anti-inflammatory compound an decycloxygenase (COX) inhibitor.
References Moser, P. et al.: J. Med. Chem., 33, 2358 (1990); Encinas, S. et al.: Photochem. Photobiol., 68,640 (1998); Kenny, J. R., et al.: J. Med. Chem., 47, 2816 (2004), Sasaki, A., et al.: J. Pharmacol. Sci., 108, 266 (2008), Dalvie, D., et al.: Chem. Res. Toxicol., 22, 357 (2009),Fórmula:C12H9Cl2NCor e Forma:WhitePeso molecular:238.112,6-Dichloro-N-phenylaniline
CAS:Fórmula:C12H9Cl2NPureza:98%Cor e Forma:Solid, White to greyish yellow green powderPeso molecular:238.11N-(2,6-Dichlorophenyl)aniline-13C6
CAS:Produto ControladoApplications N-(2,6-Dichlorophenyl)aniline-13C6 is an intermediate in the synthesis of Diclofenac-13C6 (D436449). Diclofenac-13C6 is a labelled analogue of Diclofenac Acid (D436465), which is a nonsteroidal anti-inflammatory compound and decycloxygenase (COX) inhibitor. Diclofenac-13C6 is also an intermediate in synthesizing Diclofenac-13C6 Sodium Salt (D436453), which is a labelled analogue of Diclofenac Sodium Salt (D436450).
References Yagi, K., et. al.: Biol. Pharm. Bull., 37, 1234 (2014); Kenny, J. R., et al.: J. Med. Chem., 47, 2816 (2004); Sasaki, A., et al.: J. Pharmacol. Sci., 108, 266 (2008); Dalvie, D., et al.: Chem. Res. Toxicol., 22, 357 (2009); Kenny, J. R., et al.: J. Med. Chem., 47, 2816 (2004), Sasaki, A., et al.: J. Pharmacol. Sci., 108, 266 (2008); Dalvie, D., et al.: Chem. Res. Toxicol., 22, 357 (2009)Fórmula:C6C6H9Cl2NCor e Forma:NeatPeso molecular:244.069(2,6-Dichlorophenyl)phenylamine
CAS:2,6-Dichlorophenylphenylamine is a triazine compound that has been shown to inhibit the efflux pump in bladder cells. This inhibition leads to an increase in intracellular chloride concentrations and an increase in the amount of 2,6-dichlorophenylphenylamine that is retained by the cell. The 2,6-dichlorophenylphenylamine inhibits the production of prostaglandins and other inflammatory mediators by inhibiting cyclooxygenase enzymes in the arachidonic acid pathway. 2,6-Dichlorophenylphenylamine also inhibits prostaglandin synthesis by competing with AA for acylation reactions catalyzed by acyltransferase enzymes. This leads to a decrease in the production of substances such as leukotrienes and thromboxanes. 2,6-Dichlorophenylphenylamine may be used to treat eye disorders associated withFórmula:C12H9Cl2NPureza:Min. 95%Peso molecular:238.11 g/mol2,6-Dichlorodiphenylamine
CAS:2,6-Dichlorodiphenylamine shows activity against Candida albicans infections. 2,6-Dichlorodiphenylamine elevated the MIC by 4-fold of diclofenac sodium (DFNa).Fórmula:C12H9Cl2NPureza:99.81%Cor e Forma:Off White To Cream Coloured Crystalline SolidPeso molecular:238.11










