25174-15-6

Basic information

• Product Name: 2-Propen-1-one, 3-[(4-methoxyphenyl)amino]-1-phenyl-, (2Z)-
• CAS NO: 25174-15-6
• Molecular Formula: C16H15NO2
• Molecular Weight: 253.301
• Mol File: 25174-15-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 3-[(4-methoxyphenyl)amino]-1-phenyl-, (2Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 3-[(4-methoxyphenyl)amino]-1-phenyl-, (2Z)-(25174-15-6)
• EPA Substance Registry System: 2-Propen-1-one, 3-[(4-methoxyphenyl)amino]-1-phenyl-, (2Z)-(25174-15-6)

Safety Data

• Hazardous Substances Data: 25174-15-6(Hazardous Substances Data)

Upstream product

• 89530-34-7 1-phenyl-3-trimethylsilylprop-2-yn-1-ol 
• 104-94-9 4-methoxy-aniline 
• 5437-98-9 4'-methoxyacetoacetanilide 
• 4187-87-5 1-Phenyl-2-propyn-1-ol 
• 98-86-2 acetophenone 
• 1201-93-0 1-phenyl-3-dimethylaminoprop-2-enone 
• 3623-15-2 phenyl propargyl ketone 
• 41125-10-4 benzoylacetaldehyde sodium salt 
• 20265-97-8 p-anisidine hydrochloride 
• 93-55-0 1-phenyl-propan-1-one 

Downstream Products

• 1242517-16-3 (1-(4-methoxyphenyl)-4-(thiophen-2-yl)-1,4-dihydropyridine-3,5-diyl)bis(phenylmethanone) 
• 1242517-14-1 (1-(4-methoxyphenyl)-4-p-tolyl-1,4-dihydropyridine-3,5-diyl)bis(phenylmethanone) 
• 1242517-12-9 (4-(4-chlorophenyl)-1-(4-methoxyphenyl)-1,4-dihydropyridine-3,5-diyl)bis(phenylmethanone) 
• 5455-87-8 4-methoxy-N-(4-nitrobenzylidene)aniline 
• 1242517-05-0 (1-(4-methoxyphenyl)-4-(4-nitrophenyl)-1,4-dihydropyridine-3,5-diyl)bis(phenylmethanone) 
• 1242517-13-0 (1-(4-methoxyphenyl)-4-phenyl-1,4-dihydropyridine-3,5-diyl)bis(phenylmethanone) 
• 1242517-15-2 (1,4-bis(4-methoxyphenyl)-1,4-dihydropyridine-3,5-diyl)bis(phenylmethanone) 
• 1434474-99-3 (1-(4-methoxyphenyl)-6-methyl-4,6-diphenyl-1,6-dihydropyridin-3-yl)(phenyl)methanone 

Relevant articles and documents

A Metal- and Azide-Free Multicomponent Assembly toward Regioselective Construction of 1,5-Disubstituted 1,2,3-Triazoles

The construction of 1,5-disubstituted 1,2,3-triazoles has been effected through the cascade dual C-N bond formation, N-N bond formation and an acyl migration-based C-C bond formation via the three-component reactions of enaminones, tosylhydrazine and prim

Fe-Catalyzed enaminone synthesis from ketones and amines

We have developed an iron-catalyzed direct olefination for enaminone synthesis, with saturated ketones as a source of olefins. This direct ketone β-functionalization reaction has readily available starting materials and a wide range of substrates and requires mild reaction conditions.

Water-promoted synthesis of enaminones: Mechanism investigation and application in multicomponent reactions

Highly stereoselective synthesis of Z-enaminones bearing reactive secondary amino group has been successfully performed in water using tertiary amino group functionalized enaminones under ambient conditions. An interesting promotion effect of water on the