144459-98-3

Basic information

• Product Name: 5-methylcarbonyl-4-phenyl-6-methyl-3,4-dihydropyrimidin-2(1H)-thione
• CAS NO: 144459-98-3
• Molecular Weight: 246.333
• Mol File: 144459-98-3.mol
• Article Data: 85

Chemical Properties

• CAS DataBase Reference: 5-methylcarbonyl-4-phenyl-6-methyl-3,4-dihydropyrimidin-2(1H)-thione(CAS DataBase Reference)
• NIST Chemistry Reference: 5-methylcarbonyl-4-phenyl-6-methyl-3,4-dihydropyrimidin-2(1H)-thione(144459-98-3)
• EPA Substance Registry System: 5-methylcarbonyl-4-phenyl-6-methyl-3,4-dihydropyrimidin-2(1H)-thione(144459-98-3)

Safety Data

• Hazardous Substances Data: 144459-98-3(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 17356-08-0 thiourea 
• 123-54-6 acetylacetone 
• 4756-05-2 thioacetone 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 1425352-70-0 6-acetyl-7-methyl-5-phenyl-5H-[1,3]thiazolo[3,2-a]pyrimidine-3(2H)-one hydrochloride 
• 1421829-29-9 1-(2-(4-chlorophenylthio)-4-methyl-6-phenylpyrimidin-5-yl)ethanone 
• 1420034-64-5 1-(3-butyl-7-methyl-5-phenyl-5H-thiazolo[3,2-a]pyrimidin-6-yl)ethanone 
• 1408331-88-3 1-(6-methyl-4-phenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5yl)-3-(2-methoxyphenyl)-prop-2en-1-one 
• 1408331-79-2 2-(1-(6-methyl-4-phenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-yl)ethylidene)malononitrile 
• 1408331-93-0 5-(5-(2-methoxyphenyl)-1-phenyl-1H-pyrazol-3-yl)-6-methyl-4-phenyl-1,2,3,4-tetrahydropyrimidine-2(1H)-thione 
• 1408331-73-6 2-((5-acetyl-6-methyl-4-phenyl-1,2,3,4-tetrahydropyrimidine-2yl)sulfanyl)acetic acid 
• 1400767-16-9 C₃₂H₂₄N₂O₅S 
• 1400767-15-8 C₃₆H₃₆N₂O₇S 
• 1400767-14-7 C₄₄H₃₆N₂O₃S 
• 1400767-13-6 C₃₂H₂₈N₂O₃S 
• 1400767-12-5 C₃₀H₂₂F₂N₂OS 
• 1400767-11-4 C₃₀H₂₂Br₂N₂OS 
• 1400767-10-3 C₃₀H₂₂Cl₂N₂OS 

Relevant articles and documents

Propane phosphonic acid anhydride: a new promoter for the one-pot Biginelli synthesis of 3,4-dihydropyrimidin-2(1H)-ones

Propane phosphonic acid anhydride has been found to promote the Biginelli synthesis of 3,4-dihydropyrimidin-2(1H)-ones. The use of this agent is characterized by moderate costs, low toxicity and simple workup conditions.

A green approach to synthesize dihydropyrimidinone derivatives by using anhydrous ZnCl2 catalyst under refluxing condition in heptane-toluene medium via Biginelli reaction

Aldehydes, 1a-g (1a, Ar = 4-Cl-C6H4, 1b, Ar = 4-CH3-C6H4, 1c, Ar = 2-Cl-C6H4, 1d, Ar = 2-CH3-C6H4, 1e, Ar = -C6H5, Ar = 4-Cl-C6/

Synthesis and characterization of nano acid catalyst derived from rice husk silica and its application for the synthesis of 3,4-dihydropyrimidinones/thiones compounds

In the present work, the extraction of silica nanoparticles from the rice husk followed by the modification using an acidic ionic liquid containing imidazolium butyl sulfonic acid through a sol-gel method (RH@[SiPrImBuSO3H]Cl) has been investig

A Cu(II) metal-organic framework with significant H2 and CO2 storage capacity and heterogeneous catalysis for the aerobic oxidative amination of C(sp3)-H bonds and Biginelli reactions

A Cu(ii) metal-organic framework, {[Cu2(L)(H2O)2]·(5DMF)(4H2O)}n (1), has been synthesized using an angular tetracarboxylic acid ligand (H4L) incorporating both trifluoromethyl (-CF3/