212626-89-6

Basic information

• Product Name: 2-(2-bromophenyl)-2-methylpropionaldehyde
• Synonyms: 2-(2-bromophenyl)-2-methylpropionaldehyde
• CAS NO: 212626-89-6
• Molecular Weight: 227.101
• Mol File: 212626-89-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-(2-bromophenyl)-2-methylpropionaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-bromophenyl)-2-methylpropionaldehyde(212626-89-6)
• EPA Substance Registry System: 2-(2-bromophenyl)-2-methylpropionaldehyde(212626-89-6)

Safety Data

• Hazardous Substances Data: 212626-89-6(Hazardous Substances Data)

Upstream product

• 57775-06-1 2-(2-bromophenyl)-2-methylpropanenitrile 
• 177748-63-9 methyl 2-(2-bromophenyl)-2-methylpropanoate 
• 177748-64-0 2-(2-bromophenyl)-2-methylpropan-1-ol 

Downstream Products

• 1069114-53-9 2-(2-bromophenyl)-N, 2-dimethylpropan-1-amine 
• 57625-74-8 methyl 2-methyl-2-phenylpropionate 
• 1206451-49-1 8,8-dimethylbicyclo[4.2.0]octa-1,3,5-trien-7-one 
• 98-83-9 isopropenylbenzene 
• 118968-15-3 2-(1,1-dimethyl-2-propenyl)benzonitrile 

Relevant articles and documents

Intramolecular Anti-Carbolithiation of Alkynes: Stereo-Directing Effect of Lithium-Coordinating Substituents

This paper presents the results of our investigations on the stereochemical course of intramolecular carbolithiation of alkynes. It is shown that the presence of a lithium-chelating propargylic substituent completely reverses the otherwise favored syn-pro

Pd-catalyzed intramolecular acylation of aryl bromides via C-H functionalization: A highly efficient synthesis of benzocyclobutenones

(Chemical Equation Presented) A new catalyst system for the intramolecular acylation of aldehydes with aryl bromides via C-H functionalization is described. The transformation is distinguished by a remarkable functional group tolerance and hence allows fo