1229610-04-1

Basic information

• Product Name: 2-(4-chloro-phenyl)-4-phenyl-quinazoline
• Synonyms: 2-(4-chloro-phenyl)-4-phenyl-quinazoline
• CAS NO: 1229610-04-1
• Molecular Weight: 316.79
• Mol File: 1229610-04-1.mol
• Article Data: 34

Chemical Properties

• CAS DataBase Reference: 2-(4-chloro-phenyl)-4-phenyl-quinazoline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-chloro-phenyl)-4-phenyl-quinazoline(1229610-04-1)
• EPA Substance Registry System: 2-(4-chloro-phenyl)-4-phenyl-quinazoline(1229610-04-1)

Safety Data

• Hazardous Substances Data: 1229610-04-1(Hazardous Substances Data)

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 2835-77-0 (2-aminophenyl)(phenyl)methanone 
• 7455-77-8 2-(4-chlorophenyl)-4(3H)-quinazolinone 
• 98-80-6 phenylboronic acid 
• 1878-66-6 4-chlorophenylacetic Acid 
• 623-03-0 4-Cyanochlorobenzene 
• 13141-38-3 2-phenylethynylaniline 
• 5176-12-5 (2-nitrophenyl)phenylmethanol 
• 607-68-1 2,4-dichloroquinazoline 
• 1885-29-6 anthranilic acid nitrile 
• 153172-72-6 4-chloro-N-(2-cyanophenyl)benzamide 
• 3958-47-2 triphenylindium 
• 119-61-9 benzophenone 
• 132401-91-3 3-(4-chlorophenyl)-1,4,2-dioxazol-5-one 

Relevant articles and documents

Efficient One-Pot Synthesis of Quinazoline and Benzopyrano[2,3-d]pyrimidine Derivatives Catalyzed by N-Bromosulfonamides

N,N,N',N'-tetrabromobenzene-1,3-disulfonamide and poly(N,N’-dibromo-N-ethyl-benzene-1,3-disulfonamide) were used as efficient catalysts for one-pot synthesis of new quinazoline derivatives from various aldehydes, 2-amino-benzophenone, and ammonium acetate

A new triazine-cored covalent organic polymer for catalytic applications

A triazine based covalent organic polymer (CC-TAPT-COP) was designed and synthesized via nucleophilic substitution reaction between 1,3,5-tris-(p-aminophenyl) triazine and cyanuric chloride under refluxing conditions with bottom-up approach. The structura

Synthesis of Quinazoline and Quinazolinone Derivatives via Ligand-Promoted Ruthenium-Catalyzed Dehydrogenative and Deaminative Coupling Reaction of 2-Aminophenyl Ketones and 2-Aminobenzamides with Amines

The in situ formed ruthenium catalytic system ([Ru]/L) was found to be highly selective for the dehydrogenative coupling reaction of 2-aminophenyl ketones with amines to form quinazoline products. The deaminative coupling reaction of 2-aminobenzamides with amines led to the efficient formation of quinazolinone products. The catalytic coupling method provides an efficient synthesis of quinazoline and quinazolinone derivatives without using any reactive reagents or forming any toxic byproducts.