81585-72-0

Basic information

• Product Name: Ethanone, 1-(4-bromophenyl)-2-iodo-
• CAS NO: 81585-72-0
• Molecular Formula: C8H6BrIO
• Molecular Weight: 324.944
• Mol File: 81585-72-0.mol
• Article Data: 36

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(4-bromophenyl)-2-iodo-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(4-bromophenyl)-2-iodo-(81585-72-0)
• EPA Substance Registry System: Ethanone, 1-(4-bromophenyl)-2-iodo-(81585-72-0)

Safety Data

• Hazardous Substances Data: 81585-72-0(Hazardous Substances Data)

Upstream product

• 4209-02-3 1-(4-bromophenyl)-2-chloroethan-1-one 
• 99-73-0 para-bromophenacyl bromide 
• 99-90-1 para-bromoacetophenone 
• 766-96-1 4-bromo-1-ethynylbenzene 
• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 1585-07-5 1-bromo-4-ethylbenzene 
• 934-95-2 1-bromo-4-(iodoethynyl)benzene 
• 5391-88-8 1-(4-bromophenyl)ethanol 

Downstream Products

• 17490-70-9 2,4-bis(4-bromophenyl)furan 
• 99-90-1 para-bromoacetophenone 
• 83806-46-6 (5-bromo-1-benzofuran-2-yl)(4-bromophenyl)methanone 
• 1220125-56-3 ethyl (E)-2-benzoyl-4-(4-bromophenyl)-4-oxobut-2-enoate 
• 1198087-72-7 1-(4-bromophenyl)-2-(5-methylfuran-2-yl)ethan-1-one 
• 131542-49-9 N-methyl-N-[4-(4-bromophenyl)-1,3-thiazole-2-yl]amine 
• 2103-94-8 4-(4-bromophenyl)-1,3-thiazol-2-amine 
• 1374602-40-0 3-(methoxycarbonyl)-3[2-(4-bromophenyl)-2-oxoethyl]-5-phenyl-2(3H)-furanone 
• 31377-97-6 1-(4-bromophenyl)-2-tosylethanone 
• 41024-55-9 1-(4-bromophenyl)-2-(phenylsulfonyl)ethanone 
• 140935-32-6 benzo[d]thiazol-2-yl(4-bromophenyl)methanone 
• 1394973-48-8 (4-bromophenyl)(5-chlorobenzo[d]thiazol-2-yl)methanone 
• 1609631-93-7 N-(2-(4-bromophenyl)-2-oxoacetyl)benzamide 
• 2461-83-8 1,4-bis(4-bromophenyl)-1,4-butanedione 

Relevant articles and documents

A comparison of reactivity of (EtO)2P(O)CH2I with related non-phosphorus-containing iodides in the radical iodine atom transfer addition

Based on competitive reactions and 1H NMR measurements, it was found that (EtO)2P(O)CH2I is at least 2-3 orders of magnitude less reactive than other non-phosphorus iodides of the EWG-CH2I type (EWG = NC COOMe,

Imidazolium-Based Ionic Network as a Robust Heterogeneous Catalyst in Synthesis of Phenacyl Derivatives

A new imidazolium-based poly(ionic liquid) has been synthesized and used as a robust heterogeneous catalyst for the preparation of phenacyl derivatives by an SN2 reaction of different phenacyl bromides with a broad range of nucleophiles. The products are obtained in high yields under mild conditions. The catalyst can be recycled efficiently.

Mild and General Synthesis of Pyrrolo[2,1-a]isoquinolines and Related Polyheterocyclic Frameworks from Pyrrole Precursors Derived from a Mechanochemical Multicomponent Reaction

The combination of a three-component, solvent-free pyrrole synthesis performed under mechanochemical conditions with a TMSOTf-catalyzed oxonium-mediated cyclization gave general access to pyrrolo[2,1-a]isoquinoline derivatives under very mild conditions.