139592-64-6

Basic information

• Product Name: Benzeneacetic acid, 2-bromo-a-2-propenyl-, methyl ester
• CAS NO: 139592-64-6
• Molecular Formula: C12H13BrO2
• Molecular Weight: 269.138
• Mol File: 139592-64-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzeneacetic acid, 2-bromo-a-2-propenyl-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetic acid, 2-bromo-a-2-propenyl-, methyl ester(139592-64-6)
• EPA Substance Registry System: Benzeneacetic acid, 2-bromo-a-2-propenyl-, methyl ester(139592-64-6)

Safety Data

• Hazardous Substances Data: 139592-64-6(Hazardous Substances Data)

Upstream product

• 18698-97-0 ortho-bromophenylacetic acid 
• 57486-69-8 methyl 2-(2-bromophenyl)acetate 
• 106-95-6 allyl bromide 

Downstream Products

• 139592-68-0 3-(o-bromophenyl)-2-methylhex-5-en-2-ol 
• 1254366-86-3 2-(2-bromophenyl)pent-4-enal 
• 139592-66-8 4-(o-bromophenyl)-5-iodopent-1-ene 
• 139592-67-9 4-(o-bromophenyl)pent-1-ene 
• 4175-53-5 trans-1,3-dimethyl-indane 
• 14815-73-7 methyl allylphenylacetate 
• 139592-65-7 2-(o-bromophenyl)pent-4-en-1-ol 

Relevant articles and documents

Dual Activation of Unsaturated Amides with Schwartz's Reagent: A Diastereoselective Access to Cyclopentanols and N,O-Dimethylcyclopentylhydroxylamines.

The diastereoselective access to cyclopentanols and N,O-dimethylcyclopentylhydroxylamines from 4-pentenoic acid-derived Weinreb amides is described. Based on the concomitant generation of both the nucleophilic and the electrophilic poles by hydrozirconati

The Stereochemistry of Ring Closure of Some Monosubstituted o-(But-3-enyl)phenyl Radicals

The rates and diastereoselectivity of cyclization of o-(but-3-enyl)phenyl radicals bearing substituents on the 1- or 2-position of the side chain have been examined. 1-Substituted radicals afford only 1,5-cyclization products, but 2-substituted radicals a