13573-34-7

Basic information

• Product Name: Pyrimidine, 4-(4-nitrophenyl)-2,6-diphenyl-
• CAS NO: 13573-34-7
• Molecular Formula: C22H15N3O2
• Molecular Weight: 353.38
• Mol File: 13573-34-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Pyrimidine, 4-(4-nitrophenyl)-2,6-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrimidine, 4-(4-nitrophenyl)-2,6-diphenyl-(13573-34-7)
• EPA Substance Registry System: Pyrimidine, 4-(4-nitrophenyl)-2,6-diphenyl-(13573-34-7)

Safety Data

• Hazardous Substances Data: 13573-34-7(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 100-19-6 (4-nitrophenyl)ethanone 
• 20432-02-4 1-(4-nitro-phenyl)-3-phenyl-propenone 
• 613-92-3 N-hydroxybenzenecarboximidamide 
• 1670-14-0 benzamidine monohydrochloride 
• 555-16-8 4-nitrobenzaldehdye 
• 98-86-2 acetophenone 
• 5697-42-7 dimethyl(4-nitrobenzoylmethyl)sulfonium bromide 
• 100-47-0 benzonitrile 

Relevant articles and documents

Direct synthesis of 2,4,5-trisubstituted imidazoles and di/tri-substituted pyrimidines via cycloadditions of α,β-unsaturated ketones/aldehydes and N′-hydroxyl imidamides

An efficient route for the synthesis of 5-acetylimidazoles and di/trisubstituted pyrimidines via iron-catalyzed cross-dehydrogenative coupling (CDC), with excellent tolerance and yields, has been developed. In this report, α,β-unsaturated aldehydes/ketones and N′-hydroxyl imidamides undergo [3+2] and [3+3] cycloadditions in two processes, involving iron-mediated Michael reaction, Robinson Annulation and 1,5-electrocyclization.

Preparation method of 2,4,6-triaryl-substituted-pyrimidine compounds

The invention discloses a preparation method of 2,4,6-triaryl-substituted-pyrimidine compounds. The preparation method includes the following steps that aromatic aldehyde compounds shown in the formula (I), aromatic ketone compounds shown in the formula (

Secondary amines immobilized inside magnetic mesoporous materials as a recyclable basic and oxidative heterogeneous nanocatalyst for the synthesis of trisubstituted pyrimidine derivatives

A novel magnetic MCM-41 nanocomposite-based catalyst is reported for the first time in the multicomponent synthesis of trisubstituted pyrimidines in which piperazine is immobilized inside the mesochannels of magnetic MCM-41 as an organic base (α-Fe2