1430809-05-4

Basic information

• Product Name: 3-chloro-6-phenylindolo[1,2-c]quinazoline
• Synonyms: 3-chloro-6-phenylindolo[1,2-c]quinazoline
• CAS NO: 1430809-05-4
• Molecular Weight: 328.801
• Mol File: 1430809-05-4.mol

Chemical Properties

• CAS DataBase Reference: 3-chloro-6-phenylindolo[1,2-c]quinazoline(CAS DataBase Reference)
• NIST Chemistry Reference: 3-chloro-6-phenylindolo[1,2-c]quinazoline(1430809-05-4)
• EPA Substance Registry System: 3-chloro-6-phenylindolo[1,2-c]quinazoline(1430809-05-4)

Safety Data

• Hazardous Substances Data: 1430809-05-4(Hazardous Substances Data)

Upstream product

• 1415639-49-4 C₁₄H₉BrClN 
• 1670-14-0 benzamidine monohydrochloride 
• 1211-35-4 2-(4-chlorophenyl)-1H-indole 
• 19226-36-9 3-phenyl-5H-1,4,2-dioxazol-5-one 

Relevant articles and documents

Rh(III)-Catalyzed C-H Amidation of 2-Arylindoles with Dioxazolones: A Route to Indolo[1,2-c]quinazolines

Rhodium(III)-catalyzed C-H amidation of 2-arylindoles with dioxazolones for the synthesis of indolo[1,2-c]quinazolines is reported. The reaction is compatible with a wide range of electronically diverse 2-arylindoles and dioxazolones, providing indolo[1,2

Copper-catalyzed cascade synthesis of 1H-indolo[1,2-c]quinazoline derivatives

A simple, efficient and practical approach to 1H-indolo[1,2-c]quinazoline derivatives has been developed that uses inexpensive and readily-available catalyst and substrates. The method should provide a new strategy for N-fused heterocycles and will show wide application in organic chemistry and medicinal chemistry. A simple, efficient and practical approach to 1H-indolo[1,2-c] quinazoline derivatives has been developed that uses inexpensive and readily-available catalyst and substrates. The method should provide a new strategy for N-fused heterocycles and will show wide application in organic chemistry and medicinal chemistry. Copyright