77123-53-6

Basic information

• Product Name: 6-(3-bromophenyl)benzo[4,5]imidazo[1,2-c]quinazoline
• Synonyms: 6-(3-bromophenyl)benzo[4,5]imidazo[1,2-c]quinazoline
• CAS NO: 77123-53-6
• Molecular Weight: 374.239
• Mol File: 77123-53-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-(3-bromophenyl)benzo[4,5]imidazo[1,2-c]quinazoline(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(3-bromophenyl)benzo[4,5]imidazo[1,2-c]quinazoline(77123-53-6)
• EPA Substance Registry System: 6-(3-bromophenyl)benzo[4,5]imidazo[1,2-c]quinazoline(77123-53-6)

Safety Data

• Hazardous Substances Data: 77123-53-6(Hazardous Substances Data)

Upstream product

• 15728-51-5 2-phenyl-1-p-toluenesulfonylbenzimidazole 
• 3132-99-8 m-bromobenzoic aldehyde 
• 5805-39-0 2-(aminophenyl)benzimidazole 

Downstream Products

• 77123-66-1 6-(3-ethynylphenyl)benzimidazoquinazoline 
• 77123-65-0 6-<3-<(trimethylsilyl)ethynyl>phenyl>benzimidazoquinazoline 

Relevant articles and documents

Rh(III)-Catalyzed One-Pot Synthesis of Benzimidazoquinazolines via C-H Amidation-Cyclization of N-LG-2-phenylbenzoimidazoles

An efficient protocol to synthesize substituted benzo[4,5]imidazo[1,2-c]quinazolines starting from N-LG-2-phenylbenzoimidazole and dioxazolones catalyzed by Rh(III) or Ir(III) has been developed. Various substituted benzo[4,5]imidazo[1,2-c]quinazolines co

Facile Synthesis of Ethynylated Benzoic Acid Derivatives and Aromatic Compounds via Ethynyltrimethylsilane

The coupling reaction between an aromatic halide and ethynyltrimethylsilane under the catalysis of palladium(0) generated in situ, followed by treatment of the (trimethylsilyl)ethynyl product with potassium carbonate in methanol at ambient temperatures, provides a simple approach to various ethynylated benzoic acid derivatives and other aromatic compounds.The conditions for the removal of the trimethylsilyl group were very mild, so that base-sensitive functionalities on the aromatic moiety could be tolerated.