1426902-84-2

Basic information

• Product Name: ethyl 3-[({[(E)-4-chlorobenzylidene]amino}oxy)methyl]-6-methyl-2-oxo-4-(4-methoxyphenyl)-1,2,3,4-tetrahydropyrimidine-5-carboxylate
• CAS NO: 1426902-84-2
• Molecular Weight: 457.914
• Mol File: 1426902-84-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl 3-[({[(E)-4-chlorobenzylidene]amino}oxy)methyl]-6-methyl-2-oxo-4-(4-methoxyphenyl)-1,2,3,4-tetrahydropyrimidine-5-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3-[({[(E)-4-chlorobenzylidene]amino}oxy)methyl]-6-methyl-2-oxo-4-(4-methoxyphenyl)-1,2,3,4-tetrahydropyrimidine-5-carboxylate(1426902-84-2)
• EPA Substance Registry System: ethyl 3-[({[(E)-4-chlorobenzylidene]amino}oxy)methyl]-6-methyl-2-oxo-4-(4-methoxyphenyl)-1,2,3,4-tetrahydropyrimidine-5-carboxylate(1426902-84-2)

Safety Data

• Hazardous Substances Data: 1426902-84-2(Hazardous Substances Data)

Upstream product

• 3717-24-6 4-chlorobenzaldehyde oxime 
• 161374-07-8 ethyl 4-(4-methoxyphenyl)-6-methyl-1,2,3,4-tetrahydropyrimidin-2-one-5-carboxylate 

Relevant articles and documents

Efficient synthesis of arylaldehyde oxime ethers functionalised with 3,4-dihydropyrimidinones and 2,5-quinazolinediones via a one-pot two-step method

New arylahdehyde oxime ethers functionalised with N3-3,4- dihydropyrimidinone and 2,5-quinazolinedione groups were synthesised in moderate to good yields by the reaction of the corresponding 3,4-dihydropyrimidinones and quinazolinediones with paraformaldehyde and arylaldehyde oximes via a one-pot two-step strategy in the presence of chlorotrimethylsilane. The advantages of this method are the simple procedure, the high regioselectivity of the products and the mild reaction conditions.