1146543-04-5

Basic information

• Product Name: 1-[2-(2,2-dibromo-vinyl)-phenyl]-1H-pyrrole
• Synonyms: 1-[2-(2,2-dibromo-vinyl)-phenyl]-1H-pyrrole
• CAS NO: 1146543-04-5
• Molecular Weight: 327.018
• Mol File: 1146543-04-5.mol

Chemical Properties

• CAS DataBase Reference: 1-[2-(2,2-dibromo-vinyl)-phenyl]-1H-pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[2-(2,2-dibromo-vinyl)-phenyl]-1H-pyrrole(1146543-04-5)
• EPA Substance Registry System: 1-[2-(2,2-dibromo-vinyl)-phenyl]-1H-pyrrole(1146543-04-5)

Safety Data

• Hazardous Substances Data: 1146543-04-5(Hazardous Substances Data)

Upstream product

• 253684-24-1 1-(2,2-dibromovinyl)-2-nitrobenzene 
• 552-89-6 2-nitro-benzaldehyde 
• 696-59-3 cis,trans-2,5-dimethoxytetrahydrofuran 
• 167558-54-5 2-(2,2-dibromo-vinyl)-phenylamine 

Downstream Products

• 1146543-16-9 4-(2-fluoro-4-methyl-phenyl)-pyrrolo[1,2-a]quinoline 
• 1146543-45-4 1-(2-(bromoethynyl)phenyl)-1H-pyrrole 
• 317-17-9 pyrrolo[1,2-a]quinoline 
• 1146543-18-1 4-phenethyl-pyrrolo[1,2-a]quinoline 
• 1146543-15-8 (E)-4-styryl-pyrrolo[1,2-a]quinoline 
• 1146543-12-5 4-(4-fluoro-phenyl)-pyrrolo[1,2-a]quinoline 
• 1146543-19-2 4-O-tolyl-pyrrolo[1,2-a]quinoline 
• 1146543-09-0 4-(3-chloro-phenyl)-pyrrolo[1,2-a]quinoline 
• 1146543-08-9 4-(4-chloro-phenyl)-pyrrolo[1,2-a]quinoline 
• 1146543-05-6 4-(4-methoxy-phenyl)-pyrrolo[1,2-a]quinoline 
• 796843-25-9 4-phenyl-pyrrolo[1,2-a]quinoline 
• 1146543-11-4 4-(2-fluoro-phenyl)-pyrrolo[1,2-a]quinoline 
• 1146543-06-7 4-(2-methoxy-phenyl)-pyrrolo[1,2-a]quinoline 
• 1146543-20-5 4-biphenyl-2-yl-pyrrolo[1,2-a]quinoline 

Relevant articles and documents

Palladium-Catalyzed Domino Cyclization/Phosphorylation of gem-Dibromoolefins with P(O)H Compounds: Synthesis of Phosphorylated Heteroaromatics

We presented a palladium-catalyzed domino cyclization/phosphorylation of gem-dibromoolefins, which utilize H-phosphinates and secondary phosphine oxides as the phosphine sources, respectively. A variety of phosphorylated heteroaromatics were obtained in m

Exploring the Reactivity of N-Alkynylated Sulfoximines: Acid-Catalyzed Cyclizations

N-Alkynylated sulfoximines undergo acid-promoted cyclization processes under mild reaction conditions. The transformations proceed in short reaction times affording sulfoximidoyl-functionalized naphtho[2,1-b]thiophenes or pyrrolo[1,2-a]quinolines in up to

Synthesis of pyrrolo-/indolo[1,2-a ]quinolines and naphtho[2,1- b ]thiophenes from gem -dibromovinyls and sulphonamides

A highly efficient and simple route for the synthesis of pyrrolo-/indolo[1,2-a]quinolines and naphtho[2,1-b]thiophenes from gem-dibromovinyls and sulphonamides is reported. The noteworthy feature of this report is that the methodology involves a two-step protocol to synthesize tri- and tetracyclic heterocycles in a one-pot fashion through the Cu(I)-catalyzed formation of ynamide followed by a Ag(I)-assisted intramolecular hydroarylation. The photophysical properties of representative examples of pyrrolo- and indolo[1,2-a]quinolines in solid and solution states have also been studied.

Tandem Pd-catalyzed double C-C bond formation: Effect of water

A highly efficient water-accelerated palladium-catalyzed reaction of gem-dibromoolefins with a boronic acid via a tandem Suzuki-Miyaura coupling and direct arylation is reported. A wide range of aryl, alkenyl, and alkyl boronic acids, as well as a variety