935742-52-2

Basic information

• Product Name: (2-bromophenyl)methyl (2-methylprop-2-en-1-yl) ether
• Synonyms: (2-bromophenyl)methyl (2-methylprop-2-en-1-yl) ether
• CAS NO: 935742-52-2
• Molecular Weight: 241.128
• Mol File: 935742-52-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2-bromophenyl)methyl (2-methylprop-2-en-1-yl) ether(CAS DataBase Reference)
• NIST Chemistry Reference: (2-bromophenyl)methyl (2-methylprop-2-en-1-yl) ether(935742-52-2)
• EPA Substance Registry System: (2-bromophenyl)methyl (2-methylprop-2-en-1-yl) ether(935742-52-2)

Safety Data

• Hazardous Substances Data: 935742-52-2(Hazardous Substances Data)

Upstream product

• 18982-54-2 o-bromobenzyl alcohol 
• 563-47-3 3-Chloro-2-methylpropene 
• 142820-20-0 2-methylallyl methanesulfonate 
• 1458-98-6 2-methyl-3-bromo-1-propene 

Relevant articles and documents

Domino palladium-catalyzed heck-intermolecular direct arylation reactions

A domino palladium-catalyzed Heck-intermolecular direct arylation reaction has been developed, giving access to a variety of dihydrobenzofurans, indolines, and oxindoles. A variety of sulfur-containing heterocycles such as thiazoles, thiophenes, and benzo

Synthesis of heterocycles via ligand-free palladium catalyzed reductive Heck cyclization

Synthesis of five and six membered heterocycles, indolines, 2,3-dihydrobenzofurans, chromans, isochromans, 1,2,3,4-tetrahydroquinolines, and 1,2,3,4-tetrahydroisoquinolines, in 70-99% yield by a ligand-free palladium catalyzed reductive Heck cyclization of phenyl bromides and chlorides, under mild conditions, is reported. Water was found to be essential for these reactions.