107351-82-6

Basic information

• Product Name: 2-BROMO-5-PHENYLPYRIDINE
• Synonyms: 2-BROMO-5-PHENYLPYRIDINE;Pyridine, 2-bromo-5-phenyl-
• CAS NO: 107351-82-6
• Molecular Formula: C₁₁H₈BrN
• Molecular Weight: 234.09
• Product Categories: Heterocycle-Pyridine series
• Mol File: 107351-82-6.mol
• Article Data: 21

Chemical Properties

• Melting Point: 75 °C
• Boiling Point: 335.3 ºCat 760 mmHg
• Flash Point: 156.6 ºC
• Appearance: /
• Density: 1.426 g/cm³
• Vapor Pressure: 0.000235mmHg at 25°C
• Refractive Index: 1.606
• Storage Temp.: Inert atmosphere,Room Temperature
• PKA: 0.41±0.10(Predicted)
• CAS DataBase Reference: 2-BROMO-5-PHENYLPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-5-PHENYLPYRIDINE(107351-82-6)
• EPA Substance Registry System: 2-BROMO-5-PHENYLPYRIDINE(107351-82-6)

Safety Data

• Hazardous Substances Data: 107351-82-6(Hazardous Substances Data)

Usage

General Description

2-Bromo-5-phenylpyridine is an organic compound with the chemical formula C11H8BrN. It is a brominated derivative of pyridine, a heterocyclic compound commonly found in various pharmaceuticals and agrochemicals. 2-Bromo-5-phenylpyridine is used as an intermediate in the synthesis of various pharmaceuticals, including potential antipsychotic and anticancer drugs. It is also used as a building block in the manufacture of complex organic molecules in the pharmaceutical and agrochemical industries. The compound is a solid at room temperature and is typically handled and stored under inert atmospheres to prevent degradation from air and moisture.

InChI:InChI=1/C11H8BrN/c12-11-7-6-10(8-13-11)9-4-2-1-3-5-9/h1-8H

Upstream product

• 624-28-2 2,5-dibromopyridine 
• 108-86-1 bromobenzene 
• 33421-40-8 5-phenyl-pyridin-2-ylamine 
• 591-50-4 iodobenzene 
• 225932-26-3 2-Bromo-5-(trimethylstannyl)pyridine 
• 73290-22-9 2-bromo-5-iodo-pyridine 
• 98-80-6 phenylboronic acid 
• 603-33-8 triphenylbismuthane 
• 75754-04-0 5-phenyl-pyridine-2-carboxylic acid 
• 33397-21-6 tris(4-methoxyphenyl)bismuth 
• 223463-14-7 6-bromopyridin-3-ylboronic acid 
• 20511-12-0 2-amino-5-iodopyridine 
• 504-29-0 2-aminopyridine 
• 1072-97-5 5-bromo-2-pyridylamine 

Downstream Products

• 182319-00-2 5,5'-diphenyl-2,2′-bipyridine 
• 15827-72-2 2,5-diphenylpyridine 
• 78313-67-4 5-phenyl-2-(α-thienyl)pyridine 
• 1261628-25-4 methyl 2-(5-phenylpyridin-2-yl)acetate 
• 866326-59-2 1-(5-phenylpyridin-2-yl)ethanone 

Relevant articles and documents

Aminoalkoxide-mediated formation and stabilization of phenylpyridyllithium: Straightforward access to phenylpyridine derivatives

It is shown that lithium aggregates promoted the efficient metalation of phenylpyridines and stabilization of phenylpyridyllithium. The BuLi-LiDMAE superbase prevented dimerization or nucleophilic addition encountered with t-BuLi or n-BuLi. The reported s

Synthesis of novel halopyridinylboronic acids and esters. Part 1: 6-Halopyridin-3-yl-boronic acids and esters

This paper describes a general method for the synthesis and isolation of novel 6-halo-pyridin-3-yl-boronic acids and esters 2-5. These compounds are prepared taking in account a regioselective halogen-metal exchange with a trialkylborate starting from 2,5-dihalopyridines. All substrates studied to date provided a single regioisomeric boronic acid or ester product. Additionally, these compounds have been found to undergo Pd-catalysed coupling with a range of arylhalides and authorise a strategy to produce new pyridines libraries.

Boron-containig benzopyrenes derivatives, their preparation and organic electroluminescent device (by machine translation)

The present invention relates to a 6-tritolyl-6H-6-bora benzo[cd]pyrene derivative represented by a formula (1), wherein substituents are described in an instruction. The present invention further relates to uses of the compound as an electron transportation material, and an organic electroluminescent device containing the compound. Formula (1).

Organometallic compound and organic light emitting device including the same

Disclosed are an organometallic compound and an organic light emitting device comprising the same. The organometallic compound is represented by chemical formula 1. The organic light emitting device using the organometallic compound can have a low driving