886854-01-9

Basic information

• Product Name: 4-fluoro-2-(2,2-dibromovinyl)-1-nitrobenzene
• Synonyms: 4-fluoro-2-(2,2-dibromovinyl)-1-nitrobenzene
• CAS NO: 886854-01-9
• Molecular Weight: 324.932
• Mol File: 886854-01-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 4-fluoro-2-(2,2-dibromovinyl)-1-nitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-fluoro-2-(2,2-dibromovinyl)-1-nitrobenzene(886854-01-9)
• EPA Substance Registry System: 4-fluoro-2-(2,2-dibromovinyl)-1-nitrobenzene(886854-01-9)

Safety Data

• Hazardous Substances Data: 886854-01-9(Hazardous Substances Data)

Upstream product

• 446-33-3 5-Fluoro-2-nitrotoluene 
• 558-13-4 carbon tetrabromide 
• 395-81-3 5-fluoro-2-nitrobenzaldehyde 

Downstream Products

• 59541-83-2 5-fluoro-2-phenyl-1H-indole 
• 863870-41-1 2-(2,2-dibromovinyl)-4-fluoro-phenylamine 

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

APOL1 INHIBITORS AND USE THEREOF

The invention relates to at least one compound, a deuterated derivative or a pharmaceutically acceptable salt selected from compounds of formula (I), deuterated derivatives thereof, and pharmaceutically acceptable salts thereof, compositions comprising th

A highly selective tandem cross-coupling of gem-dihaloolefins for a modular, efficient synthesis of highly functionalized indoles

(Chemical Equation Presented) A highly efficient method of indole synthesis using gem-dihalovinylaniline substrates and an organoboron reagent was developed via a Pd-catalyzed tandem intramolecular amination and an intermolecular Suzuki coupling. Aryl, alkenyl, and alkyl boron reagents are all successfully employed, making for a versatile modular approach. The reaction tolerates a variety of substitution patterns on the aniline leading to indoles with group at C2-C7. The orthogonal approach of the sequential copper- and palladium-mediated synthesis of 1,2-diarylindoles exploited the wide availability of diverse organoboron reagents.