55661-71-7

Basic information

• Product Name: Quinazoline, 1,2,3,4-tetrahydro-2-phenyl-
• CAS NO: 55661-71-7
• Molecular Formula: C14H14N2
• Molecular Weight: 210.279
• Mol File: 55661-71-7.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: Quinazoline, 1,2,3,4-tetrahydro-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Quinazoline, 1,2,3,4-tetrahydro-2-phenyl-(55661-71-7)
• EPA Substance Registry System: Quinazoline, 1,2,3,4-tetrahydro-2-phenyl-(55661-71-7)

Safety Data

• Hazardous Substances Data: 55661-71-7(Hazardous Substances Data)

Upstream product

• 1904-73-0 2-phenyl-3,4-dihydroquinazoline 
• 100-52-7 benzaldehyde 
• 4403-69-4 2-amino-1-benzylamine 
• 127896-76-8 N-(1-chlorobenzyl)pyridinium chloride 
• 895771-34-3 N-(2-aminobenzyl)benzamide 
• 1353000-46-0 2-aminobenzylamine-d2 
• 17901-93-8 benzaldehyde-d6 
• 121998-76-3 2-phenyl-2,3-dihydro-4(1H)-quinazolinone 
• 100-51-6 benzyl alcohol 

Downstream Products

• 1022-45-3 2-phenyl-4(3H)-quinazolinone 
• 1904-73-0 2-phenyl-3,4-dihydroquinazoline 
• 84570-72-9 N-(4-Nitro-phenyl)-2-(2-phenyl-1,4-dihydro-2H-quinazolin-3-yl)-propionamide 
• 84570-67-2 N-(4-Nitro-phenyl)-2-(2-phenyl-1,4-dihydro-2H-quinazolin-3-yl)-acetamide 
• 84570-70-7 N-(4-Bromo-phenyl)-2-(2-phenyl-1,4-dihydro-2H-quinazolin-3-yl)-propionamide 
• 84570-69-4 N-(4-Chloro-phenyl)-2-(2-phenyl-1,4-dihydro-2H-quinazolin-3-yl)-propionamide 
• 84570-71-8 2-(2-Phenyl-1,4-dihydro-2H-quinazolin-3-yl)-N-p-tolyl-propionamide 
• 84570-65-0 N-(4-Bromo-phenyl)-2-(2-phenyl-1,4-dihydro-2H-quinazolin-3-yl)-acetamide 
• 84570-64-9 N-(4-Chloro-phenyl)-2-(2-phenyl-1,4-dihydro-2H-quinazolin-3-yl)-acetamide 
• 84570-73-0 N-Phenyl-2-(2-phenyl-1,4-dihydro-2H-quinazolin-3-yl)-propionamide 
• 84570-66-1 2-(2-Phenyl-1,4-dihydro-2H-quinazolin-3-yl)-N-p-tolyl-acetamide 
• 84570-68-3 N-Phenyl-2-(2-phenyl-1,4-dihydro-2H-quinazolin-3-yl)-acetamide 
• 100-52-7 benzaldehyde 
• 4403-69-4 2-amino-1-benzylamine 

Relevant articles and documents

Type I ‘Lighted Metal-free’ Photosensitizing Assemblies of Phenazine for Aerobic Oxidative Transformations

Highly photostable supramolecular photosensitizing ‘lighted metal-free’ assemblies of DPZ-Th have been developed which show strong absorption in the visible region and excellent electron transportation potential from donor to acceptor units. The as-prepar

Palladium(ii): N, N, O -pincer type complex-mediated dehydrogenative coupling of alcohols to quinazolines

A new palladium(ii) N,N,O-pincer type complex-promoted one-pot cascade synthesis of quinazolines through the dehydrogenative coupling of easily available alcohols and 2-aminobenzylamine is reported. A distinct set of Pd(ii) complexes (1-2) was synthesized

Transcriptome analysis predicts mode of action of benzimidazole molecules against Staphylococcus aureus UAMS-1

Antimicrobial drug resistance is one of the most critical problems that plagued the human race in modern times. Discovery of novel antibiotics is important to counter this threat. Accordingly, herein we have reported the discovery of substituted benzimidazole class of molecules with antimicrobial property (specifically against Staphylococcus aureus). They were initially identified through a random screening and a novel catalytic synthetic strategy was utilized to access them. in vitro screening and phenotypic profiling revealed the antimicrobial nature. De novo transcriptome and gene analyses predicted the putative targets. This work provides a solid foundation for developing the benzimidazoles as a target specific antimicrobial preclinical candidate.