96583-92-5

Basic information

• Product Name: AURORA KA-6200
• Synonyms: AURORA KA-6200;CHEMPACIFIC 38172;2-AMINO-6-CHLORO-4-PHENYL-PYRIDINE-3,5-DICARBONITRILE;2-AMINO-6-CHLORO-3,5-DICYANO-4-PHENYL-PYRIDINE
• CAS NO: 96583-92-5
• Molecular Formula: C₁₃H₇ClN₄
• Molecular Weight: 254.67
• Mol File: 96583-92-5.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 496.1±45.0 °C(Predicted)
• Appearance: /
• Density: 1.43±0.1 g/cm3(Predicted)
• PKA: -4.00±0.10(Predicted)
• CAS DataBase Reference: AURORA KA-6200(CAS DataBase Reference)
• NIST Chemistry Reference: AURORA KA-6200(96583-92-5)
• EPA Substance Registry System: AURORA KA-6200(96583-92-5)

Safety Data

• Hazardous Substances Data: 96583-92-5(Hazardous Substances Data)

Upstream product

• 46177-21-3 2-benzoylmalononitrile 
• 100-52-7 benzaldehyde 
• 109-77-3 malononitrile 
• 707-07-3 orthobenzoic acid trimethyl ester 
• 67720-42-7 2-hydroxy-6-amino-4-phenylpyridine-3,5-dicarbonitrile 

Downstream Products

• 1086-02-8 2,6-dichloro-4-phenylpyridine-3,5-dicarbonitrile 
• 391663-90-4 2-amino-6-(2-hydroxyethoxy)-4-phenylpyridine-3,5-dicarbonitrile 
• 77034-27-6 6-amino-4-phenyl-2-(pyrrolidin-1-yl)-pyridine-3,5-dicarbonitrile 
• 77034-31-2 2-amino-6-(piperidin-1-yl)-4-phenylpyridine-3,5-dicarbonitrile 
• 1243606-68-9 2-amino-6-(7-azabicyclo[2.2.1]heptan-7-yl)-4-phenylpyridine-3,5-dicarbonitrile 
• 1243606-66-7 2-amino-6-(N,N-dimethylamino)-4-phenylpyridine-3,5-dicarbonitrile 
• 97118-98-4 2-amino-6-benzylamino-4-phenylpyridine-3,5-dicarbonitrile 
• 67720-42-7 2-hydroxy-6-amino-4-phenylpyridine-3,5-dicarbonitrile 
• 96461-43-7 2,6-diamino-4-phenylpyridine-3,5-dicarbonitrile 
• 1415570-60-3 C₂₉H₃₂N₆ 
• 1415570-59-0 C₂₈H₃₀N₆ 
• 1415570-58-9 C₂₇H₂₈N₆ 
• 1415570-57-8 C₂₅H₂₄N₆ 

Relevant articles and documents

Tetrachlorosilane and zinc chloride as a binary reagent for the preparation of 2-amino-6-chloropyridine-3,5-dicarbonitrile derivatives

[Figure not available: see fulltext.] A green one-pot method for efficient synthesis of 2-amino-6-chloropyridine-3,5-dicarbonitrile derivatives was developed, based on stirring of various aldehydes and malononitrile with tetrachlorosilane and zinc chloride under solvent-free conditions at room temperature for 3–10 h. The effects of zinc chloride and the reaction conditions were studied. Compounds were characterized by X-ray analysis and NMR spectroscopy.

Medicine comprising dicyanopyridine derivative

Compounds having a high conductance-type of calcium-activated K channel opening effect and a smooth muscle relaxant effect for bladder based on the K-channel opening effect, which can be used in treating pollakiuria and urinary incontinence, are provided.

Synthesis of heterocyclic compounds containing three contiguous hydrogen bonding sites in all possible arrangements

The synthesis of compounds containing three contiguous hydrogen bond sites is reported. There are six ways of arranging three adjacent hydrogen bond donor (D) and acceptor (A) sites. General synthetic routes to heterocyclic compounds with each arrangement