106910-93-4

Basic information

• Product Name: 6-isopropyl-2,4-diphenylquinazoline
• Synonyms: 6-isopropyl-2,4-diphenylquinazoline
• CAS NO: 106910-93-4
• Molecular Weight: 324.425
• Mol File: 106910-93-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-isopropyl-2,4-diphenylquinazoline(CAS DataBase Reference)
• NIST Chemistry Reference: 6-isopropyl-2,4-diphenylquinazoline(106910-93-4)
• EPA Substance Registry System: 6-isopropyl-2,4-diphenylquinazoline(106910-93-4)

Safety Data

• Hazardous Substances Data: 106910-93-4(Hazardous Substances Data)

Upstream product

• 586-61-8 4-iso-propylbromobenzene 
• 99-88-7 4-Isopropylaniline 
• 100-52-7 benzaldehyde 
• 85-44-9 phthalic anhydride 
• 118427-29-5 (4-isopropylphenyl)hydrazine hydrochloride 
• 501-65-5 diphenyl acetylene 
• 14478-73-0 3,6-diphenyl-1,4-dihydro-1,2,4,5-tetrazine 
• 95309-27-6 1,4-dihydro-1-(4-methylphenyl)-3,6-diphenyl-s-tetrazine 
• 95309-30-1 1,4-dihydro-1-isopropyl-3,6-diphenyl-s-tetrazine 
• 106910-87-6 1-(p-cumenyl)-1,4-dihydro-3,6-diphenyl-s-tetrazine 

Relevant articles and documents

Four-component quinazoline synthesis from simple anilines, aromatic aldehydes and ammonium iodide under metal-free conditions

A four-component procedure for the preparation of substituted quinazolines from anilines, aromatic aldehydes and ammonium iodide is described. The C-H bond ortho to the amino group in anilines was directly functionalized under metal-free conditions. Two a

Rearrangement Reactions of 1,3,6-Triaryl-1,4-dihydro-s-tetrazines leading to 2,4-Diarylquinazolines, 1-Anilino-3,5-diaryl-1H-1,2,4-triazoles, 1,3,5-Triaryl-1H-1,2,4-triazoles, and 2,5-Diaryl-1H-1,3,4-oxadiazoles. X-ray Structure Determination of 6-Isopropyl-2,4-diphenylquinazoline

1,3,6-Triaryl-1,4-dihydro-s-tetrazines (2c-g) rearrange on heating at ca. 200 deg C to 2,4-diarylquinazolines (for which an X-ray determination was carried out on the 6-isopropyl compound) and 1-anilino-3,5-diaryl-1H-1,2,4-triazoles as major products.Hydrolysis in chloroform solution of the title compounds (2) and their 1-alkyl analogues gives rise to 1-aryl (or alkyl)-3,5-diaryl-1H-1,2,4-triazoles and 2,5-diaryl-1,3,4-oxadiazoles.