2912-60-9

Basic information

• Product Name: α-bromophenylacetyl bromide
• Synonyms: α-bromophenylacetyl bromide
• CAS NO: 2912-60-9
• Molecular Weight: 277.943
• Mol File: 2912-60-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: α-bromophenylacetyl bromide(CAS DataBase Reference)
• NIST Chemistry Reference: α-bromophenylacetyl bromide(2912-60-9)
• EPA Substance Registry System: α-bromophenylacetyl bromide(2912-60-9)

Safety Data

• Hazardous Substances Data: 2912-60-9(Hazardous Substances Data)

Upstream product

• 103-82-2 phenylacetic acid 
• 17199-29-0 (S)-Mandelic acid 
• 103-80-0 phenylacetyl chloride 
• 4870-65-9 2-bromophenylacetic acid 
• 7436-90-0 2,2-dibromostyrene 
• 22535-03-1 phenylacetyl bromide 

Downstream Products

• 3154-09-4 1,2-Dimethoxy-4,6-bis-(α-brom-α-phenyl-acetaminomethyl)-benzol 
• 1254274-96-8 C₉H₇BrN₂S 
• 3496-32-0 phenylketene 
• 1296863-90-5 allyl 4-oxo-2,4-diphenylbutanoate 
• 99853-19-7 α-bromo phenylacetic acid allyl ester 
• 944355-52-6 2-bromo-N-(2-hydroxy-3-methylphenyl)-2-phenylacetamide 
• 944355-56-0 2-bromo-N-(2-hydroxy-4-methylphenyl)-2-phenylacetamide 
• 1186814-45-8 2-bromo-N-(2-hydroxy-5-methylphenyl)-2-phenylacetamide 
• 50552-36-8 N-Methyl-N-phenyl-α-diethylamino-phenylacetamid 
• 39982-78-0 α-bromophenylacetanilide 
• 4870-65-9 2-bromophenylacetic acid 

Relevant articles and documents

Visible light-induced intermolecular radical addition: Facile access to γ-ketoesters from alkyl-bromocarboxylates and enamines

A highly efficient addition of alkyl α-bromocarboxylates to enamines by visible light-induced photoredox catalysis is reported. Compared with traditional methods, the reaction described here provided an alternative route for the construction of valuable γ-ketoesters in generally good yields.

Liquid-phase oxidation of bromovinyl compounds with molecular oxygen

Liquid-phase oxidation of bromovinyl compounds with the aim to obtain the corresponding α-bromo acids was studied.