947232-07-7

Basic information

• Product Name: 2-(2,2-dibromovinyl)-6-methoxyphenol
• Synonyms: 2-(2,2-dibromovinyl)-6-methoxyphenol
• CAS NO: 947232-07-7
• Molecular Weight: 307.969
• Mol File: 947232-07-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-(2,2-dibromovinyl)-6-methoxyphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,2-dibromovinyl)-6-methoxyphenol(947232-07-7)
• EPA Substance Registry System: 2-(2,2-dibromovinyl)-6-methoxyphenol(947232-07-7)

Safety Data

• Hazardous Substances Data: 947232-07-7(Hazardous Substances Data)

Upstream product

• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 
• 558-13-4 carbon tetrabromide 
• 42867-45-8 (dibromomethylene)triphenylphosphorane 
• 126357-82-2 2-((tert-butyldimethylsilyl)oxy)-3-methoxybenzaldehyde 
• 947232-31-7 tert-butyl(2-(2,2-dibromovinyl)-6-methoxyphenoxy)-dimethylsilane 

Downstream Products

• 14385-51-4 7-methoxy-2-phenylbenzo[b]furan 
• 156398-61-7 (E)-2-(4-hydroxy-3-methoxyphenyl)-5-(3-hydroxyprop-1-enyl)-7-methoxybenzofuran 
• 530-22-3 egonol 
• 17375-66-5 5-(3''-hydroxypropyl)-7-methoxy-2-(3',4'-dimethoxyphenyl)benzofuran 
• 29025-30-7 7-methoxy-2-methylbenzo[b]furan 
• 1433204-70-6 C₁₅H₁₂O₂S 
• 1350910-46-1 2,3,5,6-tetrafluoro-4-(7-methoxybenzofuran-2-yl)benzonitrile 
• 92-52-4 biphenyl 

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

Copper-catalyzed synthesis of 1-(2-benzofuryl)-N-heteroarenes fromo-hydroxy-gem-(dibromovinyl)benzenes and N-heteroarenes

An efficient method for the synthesis of 1-(2-benzofuryl)-N-heteroarenes is developed fromo-hydroxy-gem-(dibromovinyl)benzenes and N-heteroarenes under copper-catalyzed tandem reaction conditions. This methodology displayed a broad substrate scope and high yields in the preparation of a variety of 1-(2-benzofuryl)-N-heteroarenes. Further, 1-(2-benzofuryl)-N-heteroarenes were also applied in the synthesis of polycyclic benzofuro-indolo-pyridine scaffolds under palladium-catalyzed dehydrogenative coupling conditions. Overall, the present tandem approach is general, synthetically advantageous and avoids air-sensitive reagents.

Intramolecular cross-coupling of gem-dibromoolefins: A mild approach to 2-bromo benzofused heterocycles

Highly useful halogenated benzofurans and benzothiophenes are prepared from readily available gem-dibromoolefins using a mild, ligand-free copper catalyzed cross-coupling procedure.