72912-33-5

Usage

Appearance

White solid

Molecular weight

281.16 g/mol

Usage

Organic synthesis and pharmaceutical research

Building block

Synthesis of biologically active molecules

Contains

Bromoethyl group and methoxybenzene group

Versatility

Modification of other organic compounds

Presence of 1,1-dimethylethoxy group

Increased stability and reduced degradation

Ideal reagent

For certain chemical reactions

Potential applications

Pharmaceutical and chemical industries

Attributes

Reactivity and stability

InChI:InChI=1/C13H19BrO2/c1-13(2,3)16-12(9-14)10-5-7-11(15-4)8-6-10/h5-8,12H,9H2,1-4H3

Upstream product

• 19484-05-0 1-((4-methoxy)phenyl)-1,2-dibromoethane 
• 75-65-0 tert-butyl alcohol 
• 637-69-4 4-Methoxystyrene 
• 100-06-1 1-(4-methoxyphenyl)ethanone 

Downstream Products

• 75306-60-4 [2-tert-Butoxy-2-(4-methoxy-phenyl)-ethyl]-[2-(2-chloro-3,4-dimethoxy-phenyl)-ethyl]-amine 
• 104113-99-7 [2-tert-Butoxy-2-(4-methoxy-phenyl)-ethyl]-[2-(3,4-dimethoxy-2-methyl-phenyl)-ethyl]-amine 
• 104113-90-8 9-Chloro-1-(4-hydroxy-phenyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine-7,8-diol; hydrobromide 
• 104113-95-3 6-Chloro-1-(4-hydroxy-phenyl)-3-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine-7,8-diol; hydrobromide 
• 104113-94-2 6-Fluoro-1-(4-hydroxy-phenyl)-3-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine-7,8-diol; hydrobromide 
• 72912-26-6 SKF 87516 hydrobromide 
• 104114-10-5 6-Fluoro-7,8-dimethoxy-1-(4-methoxy-phenyl)-1,2,4,5-tetrahydro-benzo[d]azepine-3-carbaldehyde 
• 104114-00-3 9-Chloro-7,8-dimethoxy-1-(4-methoxy-phenyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine 
• 104114-12-7 6-Fluoro-7,8-dimethoxy-1-(4-methoxy-phenyl)-3-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine 
• 104113-98-6 2-[2-(3-Chloro-4,5-dimethoxy-phenyl)-ethylamino]-1-(4-methoxy-phenyl)-ethanol 
• 77200-88-5 7,8-Dimethoxy-1-(4-methoxy-phenyl)-6-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine 
• 78495-86-0 2-[2-(3,4-Dimethoxy-2-methyl-phenyl)-ethylamino]-1-(4-methoxy-phenyl)-ethanol 
• 67287-54-1 Fenoldopam hydrobromide 
• 87863-72-7 6-chloro-2,3,4,5-tetrahydro-1-(4-hydroxyphenyl)-3-methyl-1H-3-benzazepine-7,8-diol 

Relevant academic research and scientific papers

Electrochemical Alkoxyhalogenation of Alkenes with Organohalides as the Halide Sources via Dehalogenation

A general, ideal atom utilization electrochemical technology to enable alkene alkoxyhalogenation and organohalide dehalogenation in one pot is presented. This technology is highlighted by convergent strategy integrating several reactions, such as alkene alkoxyhalogenation, organohalide dehalogenation, and dehalogenation deuteration. Experimental data suggest that alkenes have the lowest oxidation potential, which lead to anodic conversion of the C═C bond to the radical cation intermediates, and cathodic transformations of organohalides, including alkyl and aryl halides, as the nucleophilic halogen sources.

BNBTS More than brominating agent: Green and one-pot route for the C-N bond formation in water from alkenes

In this paper, in addition to introducing efficient method for bromohydrin and bromoether preparation, simple, green and efficient method to C-N bond formation from alkene and N,N'-Dibromo-N,N'-1,2-ethanediyl- bis(ptoluenesulfonamide) [BNBTS] in water was investigated. The reaction between alkenes, β-cyclodexterin, and BNBTS took place in water afterward, by making media basic; it will give the corresponding valuable building blocks in good yields (45-79%).