7025-06-1

Basic information

• Product Name: 2-BROMODIPHENYL ETHER
• Synonyms: 2-BROMODIPHENYL ETHER;(2-Bromophenyl)(phenyl) ether;(2-Bromophenyl)phenyl ether;1-Phenoxy-2-bromobenzene;2-Bromophenylphenyl ether;BDE-1;Benzene, 1-broMo-2-phenoxy-
• CAS NO: 7025-06-1
• Molecular Formula: C₁₂H₉BrO
• Molecular Weight: 249.10326
• Mol File: 7025-06-1.mol
• Article Data: 18

Chemical Properties

• Melting Point: 43.5-44.5 °C(Solv: methanol (67-56-1))
• Boiling Point: 97-100 °C(Press: 0.1 Torr)
• Appearance: /
• Density: 1.413±0.06 g/cm3(Predicted)
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 2-BROMODIPHENYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMODIPHENYL ETHER(7025-06-1)
• EPA Substance Registry System: 2-BROMODIPHENYL ETHER(7025-06-1)

Safety Data

• Hazardous Substances Data: 7025-06-1(Hazardous Substances Data)

Usage

General Description

2-Bromodiphenyl ether, also known as brominated biphenyl, is a chemical compound with the formula C12H9BrO. It is a colorless to yellow liquid with a faint, sweet odor. This chemical is primarily used as a flame retardant in various industrial and consumer products, including plastics, textiles, and electronics. It works by suppressing the combustion process, making it less likely for the material to catch fire. However, 2-Bromodiphenyl ether has been classified as a potential endocrine disruptor and may have toxic effects on aquatic organisms. Its use is regulated in some regions to minimize its environmental impact.

Upstream product

• 108-86-1 bromobenzene 
• 95-56-7 2-hydroxybromobenzene 
• 639-58-7 triphenyltin chloride 
• 958244-59-2 2-bromo-1-(2-iodophenoxy)benzene 
• 591-50-4 iodobenzene 
• 583-55-1 1-Bromo-2-iodobenzene 
• 108-95-2 phenol 
• 7732-18-5 water 
• 583-53-9 2,3-dibromobenzene 
• 71-43-2 benzene 
• 1483-73-4 diphenyliodonium bromide 
• 2688-84-8 2-phenoxyaniline 
• 66003-76-7 Diphenyliodonium triflate 
• 98-80-6 phenylboronic acid 

Downstream Products

• 104096-16-4 Bis-<2-phenoxy-phenyl>-aether 
• 183383-68-8 2-phenoxyphenyldiphenylphosphine 
• 1616098-97-5 1-(3,4-dihydroisoquinolin-2(1H)-yl)-3-((2'-phenoxy-[1,1'-biphenyl]-3-yl)oxy)propan-2-ol formate 
• 108238-09-1 2-phenoxyphenylboronic acid 

Relevant articles and documents

Side-Arm Control in Phosphine-Sulfonate Palladium- and Nickel-Catalyzed Ethylene Polymerization and Copolymerization

A series of phosphine-sulfonate ligands bearing various side-arm substituents were designed and prepared. The corresponding Pd(II) complexes [κ2-(P,O)-2-(PPhAr)-1-benzenesulfonato]Pd(Me)(dmso) (Pd1, Ar = o-MeO-C6H4; Pd2, A

Ag-Catalyzed Cyclization of Arylboronic Acids with Elemental Selenium for the Synthesis of Selenaheterocycles

A general method for the synthesis of five-membered and six-membered selenaheterocycles through Ag-catalyzed C?Se bond-forming reaction is reported. This reaction proceeds via intramolecular cyclization of arylboronic acids with selenium powder. Preliminary mechanism studies demonstrate that this transformation involves a selenium-centred radical intermediate. (Figure presented.).

Spirocyclic derivatives

The present invention provides compounds of formula (I): compositions comprising such compounds; the use of such compounds in therapy (for example in the treatment or prevention of a disease, disorder or condition ameliorated by inhibition of a dopamine transporter); and methods of treating patients with such compounds; wherein R1, R2, R3, R4, R5, R6, R9, R10, Q, X, Y, Z, A, L, B, m, n and p are as defined herein.