10352-30-4

Basic information

• Product Name: Quinoline, 2,6-dichloro-4-phenyl-
• Synonyms: 2,6-dichloro-4-phenyl-quinoline;HMS1474O13;2,6-Dichlor-4-phenylchinolin;F0016-0970
• CAS NO: 10352-30-4
• Molecular Formula: C15H9Cl2N
• Molecular Weight: 274.149
• Mol File: 10352-30-4.mol
• Article Data: 5

Chemical Properties

• Melting Point: 114-115 °C
• Boiling Point: 399.0±42.0 °C(Predicted)
• Density: 1.331±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Quinoline, 2,6-dichloro-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Quinoline, 2,6-dichloro-4-phenyl-(10352-30-4)
• EPA Substance Registry System: Quinoline, 2,6-dichloro-4-phenyl-(10352-30-4)

Safety Data

• Hazardous Substances Data: 10352-30-4(Hazardous Substances Data)

Upstream product

• 30169-33-6 6-chloro-4-phenyl-2-quinolinone 
• 30169-33-6 6-Chlor-1,2-dihydro-4-phenylchinolin-2-on 
• 962-08-3 N-(4-chlorophenyl)-3-oxo-3-phenylpropanamide 
• 719-59-5 5-chloro-2-aminobenzophenone 
• 13788-59-5 N-(2-benzoyl-4-chlorophenyl)acetamide 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 106-47-8 4-chloro-aniline 

Downstream Products

• 76093-58-8 6-Chloro-4-phenyl-2-piperazin-1-yl-quinoline 
• 1314518-56-3 (6-chloro-4-phenylquinolin-2-yl)acetonitrile 
• 1314518-72-3 C₆₈H₆₀B₂Cl₂F₄N₆O₂ 
• 1314518-65-4 C₆₈H₆₂Cl₂N₆O₂ 
• 1314518-54-1 tert-butyl (2Z)-2-[6-chloro-4-phenylquinolin-2(1H)-ylidene]-2-cyanoacetate 
• 57698-44-9 7-chloro-5-phenyl-s-triazolo<4,3-a>quinoline 
• 36916-20-8 4-(2-benzoyl-4-chlorophenyl)-5-methyl-4H-1,2,4-triazole-3-carboxaldehyde 
• 36916-19-5 5-chloro-2-(3-methyl-4H-1,2,4-triazol-4-yl)benzophenone 
• 36916-18-4 7-Chloro-1-methyl-5-phenyl-s-triazolo<4,3-a>quinoline 
• 75158-63-3 C₁₇H₁₂ClN₃O 
• 77747-14-9 2-(n-Butylamino)-6-chlor-4-phenylchinolin 
• 27537-93-5 6-chloro-2-hydrazino-4-phenylquinoline 
• 37171-92-9 2-(2-Diethylaminoethylamino)-6-chlor-4-phenylchinolin 
• 31576-98-4 6-Chlor-2-dimethylamino-4-phenylchinolin 

Relevant articles and documents

Pyrrolopyrrole cyanines: Effect of substituents on optical properties

To tune their optical properties, a large variety of pyrrolopyrrole cyanines (PPCys) were synthesized with substitutedheteroaromatics such as quinoline, benzothiazole, and oxazole derivatives as terminal groups. Thus, a broad range of stable, highly fluorescing near-infrared (NIR) dyes with high absorptivities between 690 to 845 nm is accessible. The large number of newly synthesized compounds allows a detailed discussion of the correlation between molecular structure and the optical properties of the first electronic transition. Syntheses and optical properties of pyrrolopyrrole cyanines (PPCys) with different substituents at the terminal heteroaromatic moieties are described. The relationship between molecular structure and optical properties is discussed. By suitable substitution, the absorption and fluorescence maxima of the chromophore can be tuned in a range between 690 and 845 nm. Copyright

4-Phenyl-2-(1-piperazinyl)quinolines with potent antidepressant activity

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2-[3-(Phthalimidomethyl)-5-methyl-4H-1,2,4-triazol-4-yl]benzophenones

A process to make 6-phenyl-4H-s-triazolo[4,3-a][1,4]-benzodiazepines by converting 2-[3-(hydroxymethyl)-4H-1,2,4-triazol-4-yl]benzophenones to 2-[3-[(phthalimido or methanesulfonyl)methyl]-4H-1,2,4-triazol-4-yl]benzophenones and converting these compounds to the highly active 6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepines useful as tranquilizers and sedatives.