299949-24-9

Basic information

• Product Name: ETHYL 6-METHYL-4-(4-METHYLPHENYL)-2-OXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBOXYLATE
• Synonyms: ETHYL 6-METHYL-4-(4-METHYLPHENYL)-2-OXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBOXYLATE;BUTTPARK 78\40-44;ethyl 6-methyl-2-oxo-4-(p-tolyl)-1,2,3,4-tetrahydropyrimidine-5-carboxylate
• CAS NO: 299949-24-9
• Molecular Formula: C₁₅H₁₈N₂O₃
• Molecular Weight: 274.32
• Mol File: 299949-24-9.mol
• Article Data: 112

Chemical Properties

• Melting Point: 218-219°C
• Boiling Point: 403.2±45.0 °C(Predicted)
• Appearance: /
• Density: 1.148±0.06 g/cm3(Predicted)
• PKA: 11.46±0.70(Predicted)
• CAS DataBase Reference: ETHYL 6-METHYL-4-(4-METHYLPHENYL)-2-OXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 6-METHYL-4-(4-METHYLPHENYL)-2-OXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBOXYLATE(299949-24-9)
• EPA Substance Registry System: ETHYL 6-METHYL-4-(4-METHYLPHENYL)-2-OXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBOXYLATE(299949-24-9)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 299949-24-9(Hazardous Substances Data)

Upstream product

• 589-18-4 4-Methylbenzyl alcohol 
• 141-97-9 ethyl acetoacetate 
• 57-13-6 urea 
• 104-87-0 4-methyl-benzaldehyde 
• 867372-85-8 phenyl [(p-methylphenyl)(tosyl)methyl]carbamate 
• 867372-89-2 phenyl [1-(p-methylphenyl)-2-(ethoxycarbonyl)-3-oxobutyl]carbamate 
• 41468-10-4 α-hydroxy-α-toluenesulfonate 
• 2929-93-3 p-tolylmethylenediacetate 
• 104-82-5 4-Methylbenzyl chloride 

Downstream Products

• 1239607-28-3 ethyl 1-(2-chloroacetyl)-4-methyl-2-oxo-6-p-tolyl-1,2,3,6-tetrahydropyrimidine-5-carboxylate 
• 1254330-73-8 C₂₀H₂₇N₃O₄ 
• 1254330-80-7 C₂₂H₂₄N₂O₅S 
• 1254330-81-8 C₂₃H₂₆N₂O₅S 
• 1254330-86-3 C₁₆H₁₉N₅O₃ 
• 1296205-04-3 ethyl 1-(ethoxymethyl)-4-methyl-2-oxo-6-p-tolyl-1,2,3,6-tetrahydropyrimidine-5-carboxylate 
• 854019-25-3 (R)-5-ethoxycarbonyl-6-methyl-4-(4-methylphenyl)-3,4-dihydropyrimidin-2(1H)-one 
• 854019-26-4 (S)-(+)-5-ethoxycarbonyl-6-methyl-4-(4-methylphenyl)-3,4-dihydropyrimidin-2(1H)-one 
• 1448024-26-7 (E)-ethyl 3-cinnamyl-6-methyl-2-oxo-4-p-tolyl-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 1448024-56-3 (E)-ethyl 6-methyl-2-oxo-4-p-tolyl-3-(3-p-tolylallyl)-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 1417542-44-9 ethyl 6-methyl-2-oxo-4-(4-methylphenyl)-3-[(4-phenyl-1H-1,2,3-triazol-1-yl)methyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 1417542-55-2 ethyl 6-methyl-2-oxo-4-p-tolyl-3-[(4-(4-nitrophenoxymethyl)-1H-1,2,3-triazol-1-yl)methyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 1417542-54-1 ethyl 6-methyl-2-oxo-3-[(4-pentyl-1H-1,2,3-triazol-1-yl)methyl]-4-p-tolyl-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 1395085-48-9 ethyl 2-amino-4-methyl-6-(4-methylphenyl)pyrimidine-5-carboxylate 

Relevant articles and documents

Magnetic Silica-Coated Picolylamine Copper Complex [Fe3O4@SiO2@GP/Picolylamine-Cu(II)]-Catalyzed Biginelli Annulation Reaction

An efficient and heterogeneous novel magnetic silica-coated picolylaminecopper complex [Fe3O4@SiO2@GP/Picolylamine-Cu(II)] was synthesized, characterized, and employed as a magnetically recoverable nanocatalyst in Biginelli condensation for the preparatio

Sulfonic Acid and Ionic Liquid Functionalized Covalent Organic Framework for Efficient Catalysis of the Biginelli Reaction

A quinoline-linked and ionic liquid-decorated covalent organic framework was prepared by incorporation of a multicomponent Povarov reaction and postsynthetic modification. The imidazolium and sulfonic acid-decorated COF-IM-SO3H can be a highly efficient B

A Br?nsted acidic ionic liquid anchored to magnetite nanoparticles as a novel recoverable heterogeneous catalyst for the Biginelli reaction

In this study, simple and effective methods were used for the preparation of an ionic liquid that immobilized magnetite nanoparticles. Fe3O4nanoparticles were preparedviaa chemical co-precipitation method. Then, a SiO2shel