557-95-9

Usage

Uses

Used in Pharmaceutical Industry:
Bromodiiodomethane is used as a chemical compound for addressing taste and odor events in drinking water. Its application in this industry is primarily due to its ability to mitigate the unpleasant taste and odor that may be caused by certain contaminants or natural occurrences in the water supply.
Used in Drinking Water Treatment:
In the drinking water treatment industry, Bromodiiodomethane is utilized as a component in the treatment process to improve the overall quality of the water. Its role is to help neutralize or reduce the presence of substances that may cause undesirable taste and odor, ensuring that the water is safe and palatable for consumption.

InChI:InChI=1/CHBrI2/c2-1(3)4/h1H

Upstream product

• 593-94-2 dibromoiodomethane 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 36617-02-4 1-bromo-2-phenylcyclopropane 
• 51954-37-1 1,1-Diodo-2,2-diphenylcyclopropan 
• 17343-74-7 1,1-dibromo-2,2-diphenylcyclopropane 
• 84060-81-1 1-bromo-1-iodo-2,2-diphenylcyclopropane 
• 22219-36-9 1,1-bis(4-chlorophenyl)-2,2-dibromocyclopropane 
• 84060-82-2 1-Brom-2,2-bis(4-chlorphenyl)-1-iodcyclopropan 
• 84060-83-3 1,1-Bis(4-chlorphenyl)-2,2-diiodcyclopropan 
• 63262-97-5 2,2-dibromo-1-methylcyclopropanecarbonitrile 
• 84060-84-4 2-Brom-2-iod-1-methyl-1-cyclopropancarbonitril 
• 84060-85-5 2,2-Diiod-1-methyl-1-cyclopropancarbonitril 
• 75-47-8 iodoform 
• 75-25-2 Bromoform 
• 593-94-2 dibromoiodomethane 
• 34970-00-8 bromochloroiodomethane 

Relevant academic research and scientific papers

Tandem synthesis of aromatic amides from styrenes in water

An expedient one-pot synthesis of aromatic amides has been reported from styrenes in the presence of N-bromosuccinimide and iodine by using aqueous ammonia in water. The reaction proceeds through the formation of α-bromoketone as an intermediate in the pr

Applications of Phase Transfer Catalysis, 23. Note on Bromoiodocarbene and on Pertinent Halogen Exchange Processes

A rapid halogen exchange between HCBr3, HCBr2I, HCBrI2, and HCI3 occurred in the presence of conc. sodium hydroxide and a quaternary ammonium salt.Trapping experiments with various alkenes gave cyclopropane derivatives only in 3 cases.Depending on the nucleophilicity of the alkene and the haloform, different proportions of CBr2, CBrI, and CI2 adducts were obtained.The most nucleophilic acceptor trapped those carbenes preferentially that were formed by elimination of iodide.