CAS 15307-93-4
:2,6-Dichloro-N-phenylbenzenamine
Description:
2,6-Dichloro-N-phenylbenzenamine, also known as 2,6-dichloroaniline, is an organic compound characterized by the presence of two chlorine atoms and an aniline group attached to a benzene ring. This compound typically appears as a solid at room temperature and is known for its pale yellow to light brown color. It is primarily used in the synthesis of dyes, pigments, and pharmaceuticals due to its reactivity and ability to undergo various chemical transformations. The presence of chlorine substituents enhances its electrophilic properties, making it useful in electrophilic aromatic substitution reactions. Additionally, 2,6-Dichloro-N-phenylbenzenamine may exhibit moderate toxicity, necessitating careful handling and appropriate safety measures in laboratory and industrial settings. Its solubility in organic solvents, coupled with limited water solubility, influences its applications in organic synthesis. As with many chlorinated compounds, environmental considerations regarding its persistence and potential bioaccumulation are important in assessing its overall impact.
Formula:C12H9Cl2N
InChI:InChI=1S/C12H9Cl2N/c13-10-7-4-8-11(14)12(10)15-9-5-2-1-3-6-9/h1-8,15H
InChI key:InChIKey=HDUUZPLYVVQTKN-UHFFFAOYSA-N
SMILES:N(C1=C(Cl)C=CC=C1Cl)C2=CC=CC=C2
Synonyms:- 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
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Found 13 products.
2,6-Dichlorodiphenylamine
CAS:Formula:C12H9Cl2NPurity:>98.0%(GC)Color and Shape:White to Amber to Dark green powder to crystalMolecular weight:238.11Diclofenac Impurity 1 (2,6-Dichlorodiphenylamine)
CAS:Formula:C12H9Cl2NColor and Shape:Pale Yellow SolidMolecular weight:238.112,6-Dichlorodiphenylamine
CAS:<p>2,6-Dichlorodiphenylamine</p>Purity:98%+Molecular weight:238.11g/mol2,6-Dichlorodiphenylamine
CAS:Controlled ProductFormula:C12H9Cl2NColor and Shape:NeatMolecular weight:238.11N-(2,6-Dichlorophenyl)aniline
CAS:Controlled Product<p>Applications N-(2,6-Dichlorophenyl)aniline is an analog of Diclofenac (D436450), a nonsteroidal anti-inflammatory compound an decycloxygenase (COX) inhibitor.<br>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),<br></p>Formula:C12H9Cl2NColor and Shape:WhiteMolecular weight:238.112,6-Dichloro-N-phenylaniline
CAS:Formula:C12H9Cl2NPurity:98%Color and Shape:Solid, White to greyish yellow green powderMolecular weight:238.11N-(2,6-Dichlorophenyl)aniline-13C6
CAS:Controlled Product<p>Applications 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).<br>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)<br></p>Formula:C6C6H9Cl2NColor and Shape:NeatMolecular weight:244.069(2,6-Dichlorophenyl)phenylamine
CAS:<p>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 with</p>Formula:C12H9Cl2NPurity:Min. 95%Molecular weight:238.11 g/mol2,6-Dichlorodiphenylamine
CAS:<p>2,6-Dichlorodiphenylamine shows activity against Candida albicans infections. 2,6-Dichlorodiphenylamine elevated the MIC by 4-fold of diclofenac sodium (DFNa).</p>Formula:C12H9Cl2NPurity:99.81%Color and Shape:Off White To Cream Coloured Crystalline SolidMolecular weight:238.11










