51788-87-5

Basic information

• Product Name: 2-bromo-4-fluoro-1-(prop-1-en-2-yl)benzene
• Synonyms: 2-bromo-4-fluoro-1-(prop-1-en-2-yl)benzene
• CAS NO: 51788-87-5
• Molecular Weight: 215.065
• Mol File: 51788-87-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 2-bromo-4-fluoro-1-(prop-1-en-2-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-4-fluoro-1-(prop-1-en-2-yl)benzene(51788-87-5)
• EPA Substance Registry System: 2-bromo-4-fluoro-1-(prop-1-en-2-yl)benzene(51788-87-5)

Safety Data

• Hazardous Substances Data: 51788-87-5(Hazardous Substances Data)

Upstream product

• 917-64-6 methyl magnesium iodide 
• 1006-39-9 1-(2-bromo-4-fluorophenyl)ethanone 
• 59142-68-6 2-bromo-4-fluorobenzaldehyde 
• 261711-20-0 1-(2-bromo-4-fluorophenyl)ethan-1-ol 
• 1006-41-3 2-bromo-4-fluorobenzoic acid 
• 653-92-9 methyl 2-bromo-4-fluorobenzoate 
• 51788-83-1 2-(2-bromo-4-fluorophenyl)propan-2-ol 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 1073-06-9 3-fluorobromobenzene 

Downstream Products

• 1241898-33-8 2-bromo-4-fluoro-1-(1-methylcyclopropyl)benzene 
• 1610833-58-3 3-(2-bromo-4-fluorophenyl)-3-methylcyclobutan-1-one 

Relevant articles and documents

Ene reactions of 2-borylated α-methylstyrenes: A practical route to 4-methylenechromanes and derivatives

4-Methylenechromanes were prepared via a three-step process from 2-borylated α-methylstyrenes. This sequence is based on a key glyoxylate-ene reaction catalyzed by scandium(iii) triflate. The resulting γ-hydroxy boronates, which cyclise to seven-membered

Preparation method of silicon spiro compound (by machine translation)

The invention discloses a preparation method of a silicon spiro compound. The invention provides a preparation method of a silicon spiro compound as shown in a formula II, which comprises the following steps: in a solvent, a compound represented by the formula III is subjected to cyclization reaction under the presence of a monovalent rhodium catalyst and a phosphine ligand to obtain the silicon spiro compound as shown in the formula II. The preparation method of the silicon spiro compound can be simple. , The establishment of the silicon spiro compound is realized conveniently and efficiently. (by machine translation)

Pd-Catalyzed Enantioselective Ring Opening/Cross-Coupling and Cyclopropanation of Cyclobutanones

A palladium-catalyzed enantioselective sequential ring-opening/cross-coupling of cyclobutanones is disclosed that provides chiral indanones bearing C3-quaternary stereocenters. The reaction process involves palladium-catalyzed nucleophilic addition of cyc