221539-62-4

Basic information

• Product Name: 3-(4-methoxybenzyl)-2,4-dioxo-1,2,3,4-tetrahydroquinazoline
• Synonyms: 3-(4-methoxybenzyl)-2,4-dioxo-1,2,3,4-tetrahydroquinazoline
• CAS NO: 221539-62-4
• Molecular Weight: 282.299
• Mol File: 221539-62-4.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 3-(4-methoxybenzyl)-2,4-dioxo-1,2,3,4-tetrahydroquinazoline(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-methoxybenzyl)-2,4-dioxo-1,2,3,4-tetrahydroquinazoline(221539-62-4)
• EPA Substance Registry System: 3-(4-methoxybenzyl)-2,4-dioxo-1,2,3,4-tetrahydroquinazoline(221539-62-4)

Safety Data

• Hazardous Substances Data: 221539-62-4(Hazardous Substances Data)

Upstream product

• 32315-10-9 bis(trichloromethyl) carbonate 
• 221539-30-6 2-amino-N-(4-methoxybenzyl)benzamide 
• 86-96-4 1,2,3,4-tetrahydro-quinazoline-2,4-dione 
• 824-94-2 p-methoxybenzyl chloride 
• 118-48-9 isatoic anhydride 
• 2393-23-9 4-methoxy-benzylamine 
• 530-62-1 1,1'-carbonyldiimidazole 
• 134-20-3 2-carbomethoxyaniline 
• 56651-60-6 4-methoxybenzyl isocyanate 
• 118-92-3 anthranilic acid 
• 57-13-6 urea 

Downstream Products

• 112733-34-3 2-[1,2,3,4-Tetrahydro-3-(4-methoxybenzyl)-2,4-dioxoquinazolin-1-yl]acetic acid 
• 128650-87-3 <3-(4'-hydrobenzyl)-1,2,3,4-tetrahydro-2,4-dioxo quinazolin-1-yl> acetic acid 
• 112732-92-0 Ethyl 2-[1,2,3,4-tetrahydro-3-(4-methoxybenzyl)-2,4-dioxoquinazolin-1-yl]acetate 
• 221539-88-4 1-(4-bromobutyl)-2,4-dioxo-3-(4-methoxybenzyl)-1,2,3,4-tetrahydroquinazoline 
• 221539-87-3 1-(5-chloropentyl)-2,4-dioxo-3-(4-methoxybenzyl)-1,2,3,4-tetrahydroquinazoline 

Relevant articles and documents

One-pot Syntheses of Some New 2,4(1H,3H)-quinazolinedione Derivatives in the Absence of Catalyst

A facile, rapid and one-pot procedure for the synthesis of some new 2,4(1H,3H)-quinazolinediones is described. The method involves the one-pot condensation of isatoic anhydride, primary amine and carbonyl diimidazole (CDI) in the absence of organic or inorganic catalyst. It affords the corresponding product in high yield.

Methylene chain ruler for evaluating the regioselectivity of a substrate-recognising oxidation catalyst

Regioselective C-H oxidation of aliphatic molecules with synthetic catalysts is challenging. We incorporated substrate-recognition sites into a ruthenium porphyrin-heteroaromatic N-oxide catalytic system in order to characterise its regioselectivity for t

Green synthesis of quinazolinone derivatives catalyzed by iodine in ionic liquid

A series of quinazolinone derivatives were synthesized by the reaction of 2-aminobenzamides and triethyl orthoformate or triphosgene in ionic liquid of [BMIm]BF4 at 80 °C catalyzed by iodine in good yields. Compared to other methods, this new procedure has the advantages of mild reaction conditions, good yields, operational simplicity, and environmentally friendly procedure. Copyright Taylor & Francis Group, LLC.