861374-56-3

Basic information

• Product Name: (2-bromo-allyl)-(4-bromo-phenyl)-ether
• Synonyms: (2-bromo-allyl)-(4-bromo-phenyl)-ether
• CAS NO: 861374-56-3
• Molecular Weight: 291.97
• Mol File: 861374-56-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (2-bromo-allyl)-(4-bromo-phenyl)-ether(CAS DataBase Reference)
• NIST Chemistry Reference: (2-bromo-allyl)-(4-bromo-phenyl)-ether(861374-56-3)
• EPA Substance Registry System: (2-bromo-allyl)-(4-bromo-phenyl)-ether(861374-56-3)

Safety Data

• Hazardous Substances Data: 861374-56-3(Hazardous Substances Data)

Upstream product

• 25244-30-8 4-(allyloxy)bromobenzene 
• 108244-33-3 (4-bromo-phenyl)-(2,3-dibromo-propyl)-ether 
• 106-41-2 4-bromo-phenol 
• 96-11-7 1,2,3-tribromopropane 

Downstream Products

• 33133-45-8 1-bromo-4-(prop-2-ynyloxy)benzene 

Relevant articles and documents

One-pot method for regioselective bromination and sequential carbon-carbon bond-forming reactions of allylic alcohol derivatives

An efficient one-pot method for the regioselective bromination of allylic alcohol derivatives (two-step reaction sequence) followed by Sonogashira, Negishi, or Suzuki-Miyaura coupling reactions in the same reaction vessel (three-step reaction sequence) ha

Novel one-pot method for chemoselective bromination and sequential sonogashira coupling

(Equation Presented). An efficient one-pot method for bromination- elimination of allyl alcohol derivatives and sequential Sonogashira coupling has been developed. A highlight of the method is chemoselective DBU-promoted elimination of vicinal dibromoalka

1,2-Dibromoalkanes into alkynes by elimination reaction under DBU conditions and their application to total synthesis of sapinofuranone B

Treatment of 1,2-dibromoalkanes with DBU effected an elimination reaction, leading to the alkynes. Oxygen substitution at the C3 position plays a critical role to abstract protons by inductive effects. By the application of this protocol, a total synthesi