88345-89-5

Basic information

• Product Name: 3-BROMO-4-PHENYLPYRIDINE
• Synonyms: 4-PHENYL-3-BROMOPYRIDINE;3-BROMO-4-PHENYLPYRIDINE;(3-Bromopyridin-4-yl)benzene
• CAS NO: 88345-89-5
• Molecular Formula: C₁₁H₈BrN
• Molecular Weight: 234.09
• Mol File: 88345-89-5.mol
• Article Data: 8

Chemical Properties

• Melting Point: 49-50
• Boiling Point: 293℃
• Flash Point: 131℃
• Appearance: /
• Density: 1.426
• Vapor Pressure: 0.00314mmHg at 25°C
• Refractive Index: 1.606
• CAS DataBase Reference: 3-BROMO-4-PHENYLPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMO-4-PHENYLPYRIDINE(88345-89-5)
• EPA Substance Registry System: 3-BROMO-4-PHENYLPYRIDINE(88345-89-5)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 88345-89-5(Hazardous Substances Data)

Usage

General Description

3-Bromo-4-phenylpyridine is a chemical compound with the molecular formula C11H8BrN. It is a derivative of pyridine and belongs to the class of aromatic heterocyclic compounds. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is a versatile building block in organic synthesis and can be used in the preparation of a wide range of biologically active compounds. 3-Bromo-4-phenylpyridine is also used in research and development, particularly in the pharmaceutical industry, where it is utilized in the creation of new drugs and drug candidates. Additionally, it is a valuable tool in the study of organic chemistry and serves as a key reagent in various chemical reactions.

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

Upstream product

• 89167-19-1 3-bromo-4-iodopyridine 
• 98-80-6 phenylboronic acid 
• 13534-90-2 dibromo-3,4 pyridine 
• 626-55-1 3-Bromopyridine 
• 1885-14-9 phenyl chloroformate 
• 92915-13-4 3-bromopyridinium ethylformate chloride 
• 88345-88-4 3-Bromo-4-phenyl-4H-pyridine-1-carboxylic acid phenyl ester 
• 106-51-4 p-benzoquinone 
• 90731-83-2 3-bromo-1-(phenoxycarbonyl)pyridinium chloride 

Downstream Products

• 88345-91-9 3-bromo-6-(p-methoxyphenyl)-4-phenylpyridine 
• 939-23-1 p-phenylpyridine 

Relevant articles and documents

NOVEL ORGANIC COMPOUND AND MATERIALS FOR ORGANIC ELECTROLUMINESCENT DEVICES COMPRISING THE SAME AND ORGANIC ELECTROLUMINESCENT DEVICES COMPRISING THE SAME

The present invention provides a novel organic compound represented by chemical formula 1, a material for an organic electroluminescent device including the organic compound, and an organic electroluminescent device. The present invention can improve thermal stability, color purity, and device life.

Silver-Catalyzed Minisci Reactions Using Selectfluor as a Mild Oxidant

A new method for silver-catalyzed Minisci reactions using Selectfluor as a mild oxidant is reported. Heteroarenes and quinones both participate in radical C-H alkylation and arylation from a variety of carboxylic and boronic acid radical precursors. Several oxidatively sensitive and highly reactive radical species are successful, providing structures that are challenging to access by other means.

A Pd(II)-catalyzed ring-expansion reaction of cyclic 2-azidoalcohol derivatives: Synthesis of azaheterocycles

(Chemical Equation Presented) A Pd(II)-catalyzed ring expansion-reaction of cyclic 2-azidoalcohol derivatives was found to proceed via an unprecedented C-C bond cleavage-C-N bond formation sequence, providing substituted azaheterocycles.