4783-82-8

Basic information

• Product Name: 2-(4-BROMOPHENOXY)PYRIDINE
• Synonyms: 2-(4-BROMOPHENOXY)PYRIDINE;2-(4-Bromophenoxy)pyridine 97%
• CAS NO: 4783-82-8
• Molecular Formula: C₁₁H₈BrNO
• Molecular Weight: 250.09
• Mol File: 4783-82-8.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 116 °C
• Flash Point: 148.8°C
• Appearance: /
• Density: 1.476g/cm³
• CAS DataBase Reference: 2-(4-BROMOPHENOXY)PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-BROMOPHENOXY)PYRIDINE(4783-82-8)
• EPA Substance Registry System: 2-(4-BROMOPHENOXY)PYRIDINE(4783-82-8)

Safety Data

• Hazardous Substances Data: 4783-82-8(Hazardous Substances Data)

Usage

General Description

2-(4-Bromophenoxy)pyridine is a chemical compound with the molecular formula C11H8BrNO, and it is commonly used in organic synthesis and pharmaceutical research. It is a pyridine derivative with a bromophenyl group attached to the second carbon. The compound is commonly utilized as a building block in the synthesis of various pharmaceuticals and agrochemicals. Its properties and structure make it a valuable component in the development of new compounds with potential therapeutic applications. Additionally, its bromine substituent allows for further functionalization and modification, making it a versatile intermediate for the synthesis of diverse chemical compounds.

Upstream product

• 109-04-6 2-bromo-pyridine 
• 7003-65-8 sodium 4-bromophenoxide 
• 106-41-2 4-bromo-phenol 
• 372-48-5 2-fluoropyridine 
• 95-56-7 2-hydroxybromobenzene 

Downstream Products

• 157311-66-5 3-[4-(pyridin-2-yloxy)phenyl]quinuclidin-3-ol 
• 1263099-37-1 5-(3,3-Dimethyl-but-1-ynyl)-3-[4-(pyridin-2-yloxy)-phenylamino]-thiophene-2-carboxylic acid methyl ester 
• 1309767-68-7 C₁₈H₁₁F₃N₄O 
• 1196396-14-1 2-[4-(4,4,5,5-tetramethyl-[1,3,2]-dioxaborolan-2-yl)phenoxy]pyridine 
• 1357142-47-2 1-ethyl-3-[4-(pyridin-2-yloxy)phenyl]-1H-pyrazolo[4,3-b]pyridine 
• 7693-52-9 4-bromo-2-nitrophenol 
• 2105-94-4 4-bromo-2-fluorophenol 
• 3217-15-0 4-bromo-2,6-dichloro-phenol 

Relevant articles and documents

Ruthenium-Catalyzed meta-CAr–H Bond Difluoroalkylation of 2-Phenoxypyridines

A ruthenium-catalyzed meta-selective CAr–H bond difluoroalkylation of 2-phenoxypyridine using 2-bromo-2,2-difluoroacetate has been developed. Mechanistic studies indicated that this difluoroalkylation might involve a radical process. Furthermore, a new method is reported for the synthesis of 2-(meta-difluoroalkylphenoxy)pyridine derivatives, which are present in many pharmaceuticals and other functional compounds.

IMIDAZOPYRIDINAMINE PHENYL DERIVATIVE AND USE THEREOF

The present invention relates to imidazopyridinamine phenyl derivatives, pharmaceutically acceptable salts and hydrates thereof, or metabolites thereof formed by any form of metabolism, and uses thereof in the preparation of medicaments for preventing and

A ortho-nitro phenol and its derivative synthesis method (by machine translation)

The invention relates to a method for the synthesis of organic compounds, in the existing technology of O-nitrophenol strong acid used in the synthesis process of the serious problem of environmental pollution and the synthesis step longer more complicated problem, the invention provides a ortho-nitro phenol and synthetic method of derivative thereof, proceeding by the phenol compound, synthesis of 2 - (phenoxy) pyridine, the obtained product, catalyst, tert-butyl nitrite, organic solvent and adding sealing in the pressure containers, in oil bath heating 50 - 100 °C, reaction 10 - 30 hours, to obtain 2 - (2 - nitrobenzene) ethoxy pyridine; re-processing by the ortho-nitro phenol and its derivatives; the method is simple, high-efficiency. (by machine translation)