160729-09-9

Basic information

• Product Name: 2-amino-4-(3,4-dimethoxy-phenyl)-6-phenyl-3-pyridinecarbonitrile
• Synonyms: 2-amino-4-(3,4-dimethoxy-phenyl)-6-phenyl-3-pyridinecarbonitrile
• CAS NO: 160729-09-9
• Molecular Weight: 331.374
• Mol File: 160729-09-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-amino-4-(3,4-dimethoxy-phenyl)-6-phenyl-3-pyridinecarbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-4-(3,4-dimethoxy-phenyl)-6-phenyl-3-pyridinecarbonitrile(160729-09-9)
• EPA Substance Registry System: 2-amino-4-(3,4-dimethoxy-phenyl)-6-phenyl-3-pyridinecarbonitrile(160729-09-9)

Safety Data

• Hazardous Substances Data: 160729-09-9(Hazardous Substances Data)

Upstream product

• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 98-86-2 acetophenone 
• 109-77-3 malononitrile 
• 2972-80-7 3,4-dimethoxybenzylidenemalononitrile 
• 53744-27-7 3,4-dimethoxychalcone 

Downstream Products

• 177900-50-4 2-Amino-4-(3,4-dimethoxy-phenyl)-6-phenyl-nicotinamide 

Relevant articles and documents

Experimental/computational assessments of API steel in 6 M H2SO4 medium containing novel pyridine derivatives as corrosion inhibitors

In this work, two pyridine derivatives were synthesized and explored their inhibitive influence on the API carbon steel corrosion in a 6 M H2SO4 solution. The compound was examined at different concentrations to optimized the best co

Iron(III) phosphate as a green and reusable catalyst for the synthesis of 4,6-disubstituted 2-aminopyridine-3-carbonitriles

Condensation reaction of aryl aldehydes, methyl ketones, malononitrile, and ammonium acetate in the presence of the green and recyclable catalyst FePO4 affords the corresponding 4,6-disubstituted 2-aminopyridine-3-carbonitriles. Some new derivatives of these compounds are synthesized. The catalyst can be also recycled and reused several times.

Synthesis of some new pyrimidine bases as precursors of potential anticancer nucleosides

3,5,7-Trisubstituted-pyridopyrimidine-2,4(1H,3H)-diones (4) have been synthesized from the reaction of 2-amino-3-cyano-4,6-diarylpyridines (2) with arylisocyanates in dioxan-pyridine.Compounds 4 have also been prepared by the hydrolysis of 2 with alc.KOH to give 2-amino-3-carboxamido-4,6-disubstituted pyridines (3) which on refluxing with arylisocyanate in diphenyl ether afford 4.They are characterised by elemental analyses and IR and 1H NMR spectral data.They have been tested for antibacterial and antifungal activity.