1078156-79-2

Basic information

• Product Name: ethyl 1,2-dihydro-6-methyl-2-oxo-4-(4-methylphenyl)pyrimidine-5-carboxylate
• Synonyms: ethyl 1,2-dihydro-6-methyl-2-oxo-4-(4-methylphenyl)pyrimidine-5-carboxylate
• CAS NO: 1078156-79-2
• Molecular Weight: 272.304
• Mol File: 1078156-79-2.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: ethyl 1,2-dihydro-6-methyl-2-oxo-4-(4-methylphenyl)pyrimidine-5-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1,2-dihydro-6-methyl-2-oxo-4-(4-methylphenyl)pyrimidine-5-carboxylate(1078156-79-2)
• EPA Substance Registry System: ethyl 1,2-dihydro-6-methyl-2-oxo-4-(4-methylphenyl)pyrimidine-5-carboxylate(1078156-79-2)

Safety Data

• Hazardous Substances Data: 1078156-79-2(Hazardous Substances Data)

Upstream product

• 299949-24-9 ethyl 6-methyl-2-oxo-4-p-tolyl-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 141-97-9 ethyl acetoacetate 
• 104-87-0 4-methyl-benzaldehyde 
• 57-13-6 urea 

Downstream Products

• 928152-86-7 ethyl 4-methyl-2-(piperidin-1-yl)-6-(p-tolyl)pyrimidine-5-carboxylate 
• 1245716-56-6 ethyl 4-methyl-2-morpholino-6-(p-tolyl)pyrimidine-5-carboxylate 
• 1265402-55-8 2-tert-butoxy-2-(4-methyl-2-(piperidin-1-yl)-6-p-tolylpyrimidin-5-yl)acetic acid 
• 1265402-49-0 methyl 2-tert-butoxy-2-(4-methyl-2-(piperidin-1-yl)-6-p-tolylpyrimidin-5-yl)acetate 
• 1265402-43-4 methyl 2-hydroxy-2-(4-methyl-2-(piperidin-1-yl)-6-p-tolylpyrimidin-5-yl)acetate 
• 1265402-37-6 2-(4-methyl-2-(piperidin-1-yl)-6-p-tolylpyrimidin-5-yl)-2-(trimethylsilyloxy)acetonitrile 
• 1265402-31-0 4-methyl-2-(piperidin-1-yl)-6-p-tolylpyrimidine-5-carbaldehyde 
• 1265402-25-2 (4-methyl-2-(piperidin-1-yl)-6-p-tolylpyrimidin-5-yl)methanol 
• 1245716-49-7 ethyl 4-methyl-6-p-tolyl-2-(tosyloxy)pyrimidine-5-carboxylate 

Relevant articles and documents

An electrochemical off-on method for pyrimidin-2(1: H)-one synthesis via three-component cyclization

A green and simple 'one-pot' electrochemical off-on approach to synthesize pyrimidin-2(1H)-ones was realized without any catalyst, oxidant and toxic reagent. The desired products were obtained in moderate to good yields after the stepwise 'one-pot' reacti

Palladium-catalyzed dehydrogenation of dihydro-heterocycles using isoprene as the hydrogen acceptor without oxidants

An efficient and general method for Pd-catalyzed dehydrogenative aromatization of dihydro-heteroatom compounds without external O2 and H2 is first described. The protocol firstly uses isoprene as a hydrogen acceptor. Various dihydro-

Acridone-pyrimidine hybrids- design, synthesis, cytotoxicity studies in resistant and sensitive cancer cells and molecular docking studies

Hybrid systems of acridones with substituted pyrimidines were designed with an objective of discovering next generation anticancer agents targeting multiple mechanisms in the cancer cell. Hybrid compounds were synthesized by simple and convenient methods