1256476-38-6

Basic information

• Product Name: 1-bromo-2-(but-3-en-1-yl)-4-fluorobenzene
• Synonyms: 1-bromo-2-(but-3-en-1-yl)-4-fluorobenzene
• CAS NO: 1256476-38-6
• Molecular Weight: 229.092
• Mol File: 1256476-38-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-bromo-2-(but-3-en-1-yl)-4-fluorobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-2-(but-3-en-1-yl)-4-fluorobenzene(1256476-38-6)
• EPA Substance Registry System: 1-bromo-2-(but-3-en-1-yl)-4-fluorobenzene(1256476-38-6)

Safety Data

• Hazardous Substances Data: 1256476-38-6(Hazardous Substances Data)

Upstream product

• 112399-50-5 2-bromo-5-fluorobenzyl bromide 
• 1730-25-2 allylmagnesium bromide 

Downstream Products

• 1571984-64-9 (R)-5-fluoro-1-[4-(4-methoxyphenyl)butyl]-2,3-dihydro-1H-indene 
• 1571985-16-4 (S)-5-fluoro-1-[4-(4-methoxyphenyl)butyl]-2,3-dihydro-1H-indene 
• 1571984-58-1 9-[2-(3-buten-1-yl)-4-fluorophenyl]-9-borabicyclo[3.3.1]nonane 
• 1443497-76-4 2-(but-3-en-1-yl)-4-fluorobenzaldehyde 

Relevant articles and documents

MACROCYCLIC FLU ENDONUCLEASE INHIBITORS

The present invention relates to macrocyclic pyridotriazine derivatives of formula (I) and the pharmaceutically acceptable salts, solvates or or polymorph thereof, and the use of such compounds as a medicament, in particular in the prevention and/or treatment of viral infections caused by viruses belonging to the Orthomyxoviridae famiIy. The present invention furthermore relates to pharmaceutical compositions or combination preparations of the compounds, and to the compositions or preparations for use as a medicament, more preferably for the prevention or treatment of viral infections caused by viruses belonging to the Orthomyxoviridae family.

Synthesis of five- and six-membered benzocyclic ketones through intramolecular alkene hydroacylation catalyzed by Nickel(0)/N-Heterocyclic Carbenes

Getting some closure: Mechanistic studies supported the participation of an oxanickelacycle complex in the hydroacylation step of the title reaction, which proceeds without decarbonylation even in the absence of well-known chelation assistance by heteroatoms. Copyright