3282-24-4

Basic information

• Product Name: 2-Bromo-p-terphenyl
• Synonyms: 2-Bromo-p-terphenyl;2''-Bromo-[1,1';2-Bromo-4'-phenylbiphenyl
• CAS NO: 3282-24-4
• Molecular Formula: C₁₈H₁₃Br
• Molecular Weight: 309.19982
• Mol File: 3282-24-4.mol
• Article Data: 8

Chemical Properties

• Melting Point: 85.0 to 89.0 °C
• Boiling Point: 430.5°Cat760mmHg
• Flash Point: 210.6°C
• Appearance: /
• Density: 1.309g/cm³
• Solubility: soluble in Toluene
• CAS DataBase Reference: 2-Bromo-p-terphenyl(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-p-terphenyl(3282-24-4)
• EPA Substance Registry System: 2-Bromo-p-terphenyl(3282-24-4)

Safety Data

• RIDADR: UN 3152 9/PG II
• HazardClass: 9
• PackingGroup: II
• Hazardous Substances Data: 3282-24-4(Hazardous Substances Data)

Usage

General Description

2-Bromo-p-terphenyl is a chemical compound derived from terphenyl, a hydrocarbon consisting of three benzene rings joined together. The addition of a bromine atom to the p-terphenyl molecule results in the formation of 2-Bromo-p-terphenyl, which is commonly used as a building block for the synthesis of various organic compounds. 2-Bromo-p-terphenyl has applications in the field of organic chemistry, particularly in the development of pharmaceuticals, agrochemicals, and materials science. It is valued for its versatile reactivity and ability to serve as a precursor for the creation of complex organic molecules with specific functionalities. Additionally, 2-Bromo-p-terphenyl is studied for its potential use in the development of advanced materials and as a reagent in chemical research.

Upstream product

• 108-86-1 bromobenzene 
• 857620-57-6 N-biphenyl-4-yl-N-nitroso-acetamide 
• 129112-25-0 2-(trifluoromethanesulfonyl)oxy-bromobenzene 
• 3315-91-1 4-biphenylylmagnesium bromide 
• 583-55-1 1-Bromo-2-iodobenzene 
• 5122-94-1 4-biphenylboronic acid 
• 4075-79-0 4-phenylacetanilide 

Downstream Products

• 1334287-58-9 4-(2'-p-terphenyl)benzaldehyde 
• 1632125-31-5 6-ethoxy-3-phenyl-6H-dibenz[c,e][1,2]oxaphosphorin-6-oxide 
• 663954-31-2 ([1,1':4',1''-terphenyl]-2-yl)boronic acid 
• 1615699-51-8 C₂₇H₂₅P 
• 1615699-50-7 C₂₅H₂₁P 
• 1615699-48-3 C₂₅H₂₄BP 
• 1528732-78-6 2-(cyclohepta-2,4,6-trien-1-yl)-1,1':4',1''-terphenyl 
• 28065-98-7 2-phenylfluorene 
• 1426051-51-5 bis[1,1';4',1'']terphenyl-2-yl-silane 

Relevant articles and documents

Amine compound and organic electroluminescent device including the same

An organic electroluminescence device of an embodiment includes a first electrode, a second electrode, and a plurality of organic layers disposed between the first electrode and the second electrode, wherein at least one among the plurality of organic layers includes an amine compound represented by Formula 1a, thereby showing excellent emission efficiency and/or improved life characteristics:

Palladium-catalyzed relay C–H functionalization to construct novel hybrid-arylcyclophosphorus ligand precursors

A new relay C–H functionalization of di([1,1′-biphenyl]-2-yl)phosphine oxide to obtain esterified and hydroxylated products with different hypervalent iodines as oxidants under palladium catalysis is disclosed. This reaction provides a more effective and concise strategy for the synthesis of novel structural hybrid-arylcyclophosphorus ligand precursors with a wide range of substrates and good functional group tolerance.

Intramolecular anti-Phosphinoauration of Alkynes: An FLP-Motivated Approach to Stable Aurated Phosphindolium Complexes

The synthesis of aurated phosphindolium complexes from easy accessible 1,5-alkynylphosphine derivatives has been studied by using gold(I) complexes featuring carbene and phosphine ligands as initiators. Upon formation of the mixed phosphine NHC/phosphine