52537-82-3

Basic information

• Product Name: 2-(6-chloro-4-phenylquinazoline-2-yl)phenol
• Synonyms: 2-(6-chloro-4-phenylquinazoline-2-yl)phenol
• CAS NO: 52537-82-3
• Molecular Weight: 332.789
• Mol File: 52537-82-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-(6-chloro-4-phenylquinazoline-2-yl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(6-chloro-4-phenylquinazoline-2-yl)phenol(52537-82-3)
• EPA Substance Registry System: 2-(6-chloro-4-phenylquinazoline-2-yl)phenol(52537-82-3)

Safety Data

• Hazardous Substances Data: 52537-82-3(Hazardous Substances Data)

Upstream product

• 82562-59-2 [5-Chloro-2-(2,2-dimethyl-2H-benzo[e][1,3]oxazin-4-ylamino)-phenyl]-phenyl-methanone 
• 84570-96-7 2-(6-Chloro-4-phenyl-1,2,3,4-tetrahydro-quinazolin-2-yl)-phenol 
• 719-59-5 5-chloro-2-aminobenzophenone 
• 90-02-8 salicylaldehyde 
• 74405-07-5 4-chloro-2,2-dimethyl-2H-benzo[e][1,3]oxazine 

Relevant articles and documents

Synthesis of quinazolines over recyclable Fe3O4@SiO2-PrNH2-Fe3+ nanoparticles: A green, efficient, and solvent-free protocol

A practical and efficient method is developed for efficient synthesis of quinazoline derivatives through condensation reaction of 2-aminoaryl ketone, an aldehyde, and ammonium acetate, over magnetic Fe3O4@SiO2-PrNH2/

Recyclable, magnetic ionic liquid bmim[FeCl4]-catalyzed, multicomponent, solvent-free, green synthesis of quinazolines

An atom-efficient, eco-friendly, solvent-free, high yielding, multicomponent green strategy to synthesize highly functionalized quinazoline derivatives by the one-pot reaction of 2-aminobenzophenone, aromatic aldehyde and ammonium acetate is presented. Ma

Ecofriendly and efficient one-pot procedure for the synthesis of quinazoline derivatives catalyzed by an acidic ionic liquid under aerobic oxidation conditions

A three-component condensation reaction between 2-aminobenzophenone derivatives, formaldehyde or aromatic aldehydes, and ammonium acetate efficiently provides substituted quinazolines in a one-pot reaction in the presence of Bronsted acidic ionic liquid, 1-methylimidazolium triflouroacetate ([Hmim]TFA), in conjunction with aerobic oxidation. The ionic liquid was separated from the reaction mixture by simple extraction and was recycled three times without considerable loss in activity. Copyright Taylor & Francis Group, LLC.