34883-46-0

Usage

Uses

Used in Pharmaceutical Industry:
1-IODO-2-PHENOXY-BENZENE is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new medications and therapies.
Used in Agrochemical Industry:
1-IODO-2-PHENOXY-BENZENE is used as a chemical intermediate in the production of agrochemicals, aiding in the creation of pesticides and other agricultural products to enhance crop protection and yield.
Used in Research Applications:
1-IODO-2-PHENOXY-BENZENE is utilized as a research compound for studying organic chemistry, chemical reactions, and the development of new chemical processes or products.
Used in Industrial Applications:
1-IODO-2-PHENOXY-BENZENE is used in the industrial manufacture of various products, serving as a key component in the production process due to its unique chemical properties.
It is crucial to handle and store 1-IODO-2-PHENOXY-BENZENE with proper safety measures due to its toxic and potentially harmful nature.

InChI:InChI=1/C12H9IO/c13-11-8-4-5-9-12(11)14-10-6-2-1-3-7-10/h1-9H

Upstream product

• 2688-84-8 2-phenoxyaniline 
• 101-84-8 diphenylether 
• 533-58-4 2-Iodophenol 
• 1483-73-4 diphenyliodonium bromide 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 591-50-4 iodobenzene 
• 66003-76-7 Diphenyliodonium triflate 
• 2216-12-8 1-nitro-2-phenoxy-benzene 
• 615-42-9 1,2-Diiodobenzene 
• 108-95-2 phenol 
• 26838-86-8 pyridine-2-carboxylic acid phenyl ester 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 71-43-2 benzene 
• 88-73-3 2-Chloronitrobenzene 

Downstream Products

• 2243-42-7 2-phenoxybenzoic acid 
• 5864-20-0 (2-dichloroiodanyl-phenyl)-phenyl ether 
• 2974-88-1 2,2'-diphenoxybiphenyl 
• 103859-67-2 1-iodo-2-(4-nitrophenoxy)benzene 
• 35883-08-0 2'-nitro-2-phenoxybiphenyl 
• 128039-26-9 1-(p-methoxyphenyl)-2-(o-(phenyloxy)phenyl)ethyne 
• 132-64-9 dibenzofuran 
• 101-84-8 diphenylether 
• 95161-71-0 2-o-Phenoxyphenyl-naphthalin 
• 95161-70-9 1-o-Phenoxyphenyl-naphthalin 
• 3586-12-7 3-phenoxyaniline 
• 1028267-14-2 3-(2-phenoxy-phenyl)-prop-2-yn-1-ol 
• 144836-72-6 5-iodo-6-phenyldibenzoxepine 
• 144836-71-5 E/Z-1,2-dibromo-1-(o-phenoxyphenyl)-1-phenylethene 

Relevant academic research and scientific papers

Method for preparing 2-iodo aryl ether under action of alkali metal hydride

The invention discloses a method for preparing 2-iodo aryl ether under the action of alkali metal hydride, which comprises the following steps: adding alkali metal hydride and phenol into a solvent, then adding 1, 2-diiodo aromatic hydrocarbon, and reacti

COMPOUND AND ORGANIC ELECTRONIC DEVICE USING THE SAME

Provided are a novel compound and an organic electronic device using the same. The novel compound is represented by the following Formula (I): wherein Y is an oxygen atom or a sulfur atom; X1 and X2 are each independently C(Ra), the two (Ra)s are the same or different, and the two (Ra)s are joined together to form a first aryl ring; X3 and X4 are each independently C(Rb), the two (Rb)s are the same or different, and the two (Rb)s are joined to form a second aryl ring or a heteroaryl ring.

Condensed fluorene derivative comprising heterocyclic ring

The present invention relates to a condensed fluorene derivative comprising a heterocyclic ring and, more particularly, to an intermediate product for manufacturing a heterocyclic ring compound which can show excellent luminance and luminous efficiency when used as an organic light emitting material, while exhibiting excellent element characteristics with a long lifespan.COPYRIGHT KIPO 2020

COMPOUND AND ORGANIC ELECTRONIC DEVICE USING THE SAME

Provided are a novel compound and an organic electronic device using the same. The novel corn pound is represented by the following Formula (I): wherein Y is an oxygen atom, a sulfur atom, or a sulfur dioxide group; X1 and X2 are each independently C(Ra), multiple (Ra)s are the same or different, and the two (Ra)s are joined together to form a first aryl ring; X3 and X4 are each independently C(Rb), multiple (Rb)s are the same or different, and the two (Rb)s are joined to form a second aryl ring or a heteroaryl ring.

Synthesis of medium-sized (6-7-6) ring compounds by iron-catalyzed dehydrogenative C-H activation/annulation

In this report, we have described a FeCl3-catalyzed process involving intramolecular annulation of o-phenoxy diarylacetylenes via hydroarylation to afford a series of biologically potent fused seven-membered (6-7-6) ring compounds under mild reaction conditions. This reaction was believed to proceed through Friedel-Crafts type sequential carbometallation followed by protonation to produce phenyldibenz[b,f]oxepines. This method was also extended to synthesize seven-membered rings that are fused with coumarins.

COMPOUND AND ORGANIC ELECTRONIC DEVICE USING THE SAME

Provided are a novel compound and an organic electronic device using the same. The novel compound is represented by the following Formula (I): wherein Y is an oxygen atom or a sulfur atom; X 1and X 2are each independently C(R a), the two(R a)s are the same or different, and the two (R a)s are joined together to form a first aryl ring; X 3and X 4are each independently C(R b), the two (R b)s are the same or different, and the two (R b)s are joined to form a second aryl ring or a heteroaryl ring.

Intramolecular Aryl Migration of Diaryliodonium Salts: Access to ortho-Iodo Diaryl Ethers

By using vicinal trifluoromethanesulfonate-substituted diaryliodonium salts, a novel approach was developed for the synthesis of ortho-iodo diaryl ethers by intramolecular aryl migration. The reaction conditions are mild with a broad substrate scope. Mechanistic insight suggests a sulfonyl-directed nucleophilic aromatic substitution pathway. Additionally, the product ortho-iodo diaryl ethers serve as versatile synthons as demonstrated with several coupling reactions. Furthermore, a useful thyroxine analogue of the 3-iodo-l-thyronine (3-T1) derivative was synthesized by this aryl migration procedure.

Competing Pathways in O-Arylations with Diaryliodonium Salts: Mechanistic Insights

A mechanistic study of arylations of aliphatic alcohols and hydroxide with diaryliodonium salts, to give alkyl aryl ethers and diaryl ethers, has been performed using experimental techniques and DFT calculations. Aryne intermediates have been trapped, and additives to avoid by-product formation originating from arynes have been found. An alcohol oxidation pathway was observed in parallel to arylation; this is suggested to proceed by an intramolecular mechanism. Product formation pathways via ligand coupling and arynes have been compared, and 4-coordinated transition states were found to be favored in reactions with alcohols. Furthermore, a novel, direct nucleophilic substitution pathway has been identified in reactions with electron-deficient diaryliodonium salts.

Novel compounds for organic light-emitting diode and organic light-emitting diode including the same

The present invention relates to a compound represented by chemical formula B, and an organic light-emitting device including the same. In the chemical formula B, cyclic groups A1 to A3, structural formulas Q1 and Q2, R1 and R2, L1 to L4, Ar1 to Ar4, E, and F are the same as defined in the present specification. More specifically, provided is a compound for organic light-emitting devices exhibiting excellent device properties such as low voltage driving properties and luminous efficiency.COPYRIGHT KIPO 2017

Organic light-emitting element capable of low-voltage drive and having long life

The present invention relates to an organic light-emitting element capable of low-voltage drive and also having a long life, and, more specifically, relates to an organic light-emitting element comprising: a first electrode; a second electrode facing the first electrode; and a light-emitting layer interposed between the first electrode and the second electrode, wherein the light-emitting layer comprises at least one amine compound represented by [chemical formula A] or [chemical formula B], and at least one compound represented by [chemical formula D], and the structures of [chemical formula A], [chemical formula B] and [chemical formula D] are the same as given in the detailed description of the invention.