82777-09-1

Basic information

• Product Name: 2'-Iodo-1,1':3',1''-terphenyl
• Synonyms: 2'-Iodo-1,1':3',1''-terphenyl;2-iodo-1,3-diphenylbenzene;2'-Iodo-m-terphenyl
• CAS NO: 82777-09-1
• Molecular Formula: C₁₈H₁₃I
• Molecular Weight: 356.20029
• Mol File: 82777-09-1.mol
• Article Data: 10

Chemical Properties

• Melting Point: 113-116°C
• Appearance: /
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• Sensitive: Light Sensitive
• CAS DataBase Reference: 2'-Iodo-1,1':3',1''-terphenyl(CAS DataBase Reference)
• NIST Chemistry Reference: 2'-Iodo-1,1':3',1''-terphenyl(82777-09-1)
• EPA Substance Registry System: 2'-Iodo-1,1':3',1''-terphenyl(82777-09-1)

Safety Data

• Hazardous Substances Data: 82777-09-1(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
2'-Iodo-1,1':3',1''-terphenyl is used as a building block in organic synthesis for the preparation of functional materials. Its unique structure allows for the creation of a variety of complex organic compounds, making it a valuable component in the synthesis process.
Used in Organic Electronic Devices:
2'-Iodo-1,1':3',1''-terphenyl has been studied for its potential use in organic electronic devices due to its electronic properties. Its incorporation into these devices can enhance their performance and contribute to the development of advanced electronic technologies.
Used as a Fluorescent Probe in Biological Imaging:
2'-Iodo-1,1':3',1''-terphenyl has been investigated for its potential as a fluorescent probe in biological imaging. Its fluorescent properties can be utilized to visualize and study biological processes, offering a valuable tool for researchers in the life sciences.
Used in Light-Emitting Devices:
The photophysical properties of 2'-Iodo-1,1':3',1''-terphenyl have been explored for potential applications in light-emitting devices. Its ability to emit light can be harnessed in the development of more efficient and innovative lighting technologies.

Upstream product

• 62347-12-0 2,6-dichlorophenyllithium 
• 100-58-3 phenylmagnesium bromide 
• 108-86-1 bromobenzene 
• 19821-80-8 1,3-dibromo-2-iodo-benzene 
• 98-80-6 phenylboronic acid 
• 19230-28-5 1,3-dichloro-2-iodobenzene 
• 92-06-8 1,3-diphenylbenzene 
• 591-51-5 phenyllithium 
• 541-73-1 1,3-Dichlorobenzene 
• 19625-69-5 2'-nitro[1,1';3',1'']terphenyl 
• 13402-32-9 1,3-dibromo-2-nitrobenzene 
• 87666-57-7 2,6-diphenylaniline 
• 608-30-0 2,6-dibromoaniline 

Downstream Products

• 87666-64-6 3',6''-Diphenyl-o-quaterphenyl 
• 92-52-4 biphenyl 
• 92-06-8 1,3-diphenylbenzene 
• 135-70-6 p-quaterphenyl 
• 87666-66-8 2,6-Diphenyl-p-terphenyl 
• 270083-12-0 EuI₂(thf)5 
• 270083-10-8 Eu(2,6-Ph₂C₆H₃)2(thf)2 
• 270083-11-9 Yb(2,6-Ph₂C₆H₃)2(thf)2 
• 1165-14-6 1,2,3-triphenylbenzene 
• 20199-30-8 1,4-di(1-naphthyl)butadiyne 

Relevant articles and documents

Synthesis of diiodinated biphenyls and iodinated meta-terphenyls by regioselective Suzuki-Miyaura cross-coupling reactions of 5-substituted 1,2,3-triiodobenzenes

A variety of 2,3-diiodinated biphenyl and iodinated meta-terphenyl derivatives were synthesized by a regioselective Suzuki-Miyaura cross-coupling reaction of 5-substituted 1,2,3-triiodobenzenes. By using 1 equiv. of arylboronic acid, the Suzuki-Miyaura re

Efficient Suppression of Chain Transfer and Branching via Cs-Type Shielding in a Neutral Nickel(II) Catalyst

An effective shielding of both apical positions of a neutral NiII active site is achieved by dibenzosuberyl groups, both attached via the same donors’ N-aryl group in a Cs-type arrangement. The key aniline building block is accessibl

Synthesis of α-alkylated γ-butyrolactones with concomitant anhydride kinetic resolution using a sulfamide-based catalyst

The Kinetic Resolution (KR) of α-alkylated enolisable disubstituted anhydrides has been shown to be possible for the first time. In the presence of an ad hoc designed novel class of bifunctional sulfamide organocatalyst, a regio-, diastereo- and enantioselective cycloaddition reaction between the enolisable anhydride and benzaldehydes provides densely functionalised γ-butyrolactones in one pot (up to 19:1 dr, 94% ee) with control over three contiguous stereocentres. The concomitant resolution of the starting material anhydride, provides access to a range of chiral succinate derivatives with selectivity factors up to S? = 10.5.