72912-33-5

Basic information

• Product Name: 1-[2-bromo-1-(1,1-dimethylethoxy)ethyl]-4-methoxybenzene
• Synonyms: 1-[2-bromo-1-(1,1-dimethylethoxy)ethyl]-4-methoxybenzene
• CAS NO: 72912-33-5
• Molecular Formula: C₁₃H₁₉BrO₂
• Molecular Weight: 287.19276
• EINECS: 277-013-5
• Mol File: 72912-33-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 321.6°C at 760 mmHg
• Flash Point: 122.8°C
• Appearance: /
• Density: 1.234g/cm³
• Vapor Pressure: 0.000553mmHg at 25°C
• Refractive Index: 1.517
• CAS DataBase Reference: 1-[2-bromo-1-(1,1-dimethylethoxy)ethyl]-4-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[2-bromo-1-(1,1-dimethylethoxy)ethyl]-4-methoxybenzene(72912-33-5)
• EPA Substance Registry System: 1-[2-bromo-1-(1,1-dimethylethoxy)ethyl]-4-methoxybenzene(72912-33-5)

Safety Data

• Hazardous Substances Data: 72912-33-5(Hazardous Substances Data)

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 
• 67287-53-0 6-chloro-7,8-dimethoxy-1-(4-methoxyphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine 
• 71636-38-9 N-[2-hydroxy-2-(4'-methoxyphenyl)ethyl]-2-(2-chloro-3,4-dimethoxyphenyl)ethylamine 
• 78495-91-7 6-methyl-7,8-dihydroxy-1-(4-hydroxyphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine 
• 72912-25-5 6-Fluoro-7,8-dimethoxy-1-(4-methoxy-phenyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine 
• 95413-95-9 N-<2-hydroxy-2-(4-methoxyphenyl)>-2-(3,4-dimethoxy-2-fluorophenyl)ethylamine 
• 100166-60-7 6-Chloro-7,8-dimethoxy-1-(4-methoxy-phenyl)-1,2,4,5-tetrahydro-benzo[d]azepine-3-carbaldehyde 
• 87863-72-7 6-chloro-2,3,4,5-tetrahydro-1-(4-hydroxyphenyl)-3-methyl-1H-3-benzazepine-7,8-diol 
• 67287-54-1 Fenoldopam hydrobromide 
• 78495-86-0 2-[2-(3,4-Dimethoxy-2-methyl-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 
• 104113-98-6 2-[2-(3-Chloro-4,5-dimethoxy-phenyl)-ethylamino]-1-(4-methoxy-phenyl)-ethanol 
• 104114-12-7 6-Fluoro-7,8-dimethoxy-1-(4-methoxy-phenyl)-3-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine 

Relevant articles and documents

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.

Synthesis and renal vasodilator activity of some dopamine agonist 1-aryl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diols: Halogen and methyl analogues of fenoldopam

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