25856-03-5

Basic information

• Product Name: 1,3-Propanedione, 1-(4-methoxyphenyl)-3-(4-methylphenyl)-
• CAS NO: 25856-03-5
• Molecular Formula: C17H16O3
• Molecular Weight: 268.312
• Mol File: 25856-03-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,3-Propanedione, 1-(4-methoxyphenyl)-3-(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Propanedione, 1-(4-methoxyphenyl)-3-(4-methylphenyl)-(25856-03-5)
• EPA Substance Registry System: 1,3-Propanedione, 1-(4-methoxyphenyl)-3-(4-methylphenyl)-(25856-03-5)

Safety Data

• Hazardous Substances Data: 25856-03-5(Hazardous Substances Data)

Upstream product

• 65418-72-6 1-(4-methoxyphenyl)-3-(4-methylphenyl)-2-ethynyl-1-one 
• 6552-66-5 3-(4-methoxyphenyl)-1-p-tolylprop-2-en-1-one 
• 32045-76-4 2,3-dibromo-3-(4-methoxyphenyl)-1-(4-methylphenyl)-propan-1-one 

Downstream Products

• 33425-19-3 1-(4-methoxyphenyl)-2-(4-methylphenyl)ethane-1,2-dione 
• 37613-33-5 5-(4-methoxyphenyl)-3-(p-tolyl)isoxazole 
• 193486-28-1 1-(4-methoxyphenyl)-2,2-dimethyl-3-(4-methylphenyl)-propane-1,3-dione 
• 65205-51-8 3-(4′-methoxyphenyl)-5-(4″-methylphenyl)isoxazole 
• 22693-32-9 4-methylbenzoyl azide 
• 3532-17-0 4-methoxybenzoyl azide 

Relevant articles and documents

A metal-free strategy for the cross-dehydrogenative coupling of 1,3-dicarbonyl compounds with 2-methoxyethanol

Here, we report a metal-free approach for the construction of methylene-bridged bis-1,3-dicarbonyl compounds via cross-dehydrogenative coupling of 1,3-dicarbonyl compounds with 2-methoxyethanol. In addition, we have extended this methodology to synthesize tetra-substituted pyridine derivatives using 1,3-dicarbonyl, 2-methoxyethanol and NH4OAc in one step. The key advantages include accepting a wide range of substrates, utilizing O2 as the sole oxidant, and synthesizing biologically active compounds such as 1,4-dihydropyridine and pyrazole. This journal is

Synthesis and antimicrobial activity of 1-(4-chlorophenyl)-3-(4-methoxy/3,4-dimethoxyphenyl)propan-1,3-diones and their 2-analogs

The condensation of substituted acetophenones 1-5 with 4-methoxy- or 3,4-dimethoxy-benzaldehyde (6,7) in ethanolic NaOH gives the corresponding substituted 2-propen-1-ones (8-17) which on bromination yields substituted propan-1-ones (18-27).Refluxing of 1