34883-46-0

Basic information

• Product Name: 1-IODO-2-PHENOXY-BENZENE
• Synonyms: 1-IODO-2-PHENOXY-BENZENE;Benzene, 1-iodo-2-phenoxy-;2-Iododiphenyl ether;2-Iodophenyl phenyl ether
• CAS NO: 34883-46-0
• Molecular Formula: C₁₂H₉IO
• Molecular Weight: 296.10373
• Mol File: 34883-46-0.mol
• Article Data: 27

Chemical Properties

• Melting Point: 56℃
• Boiling Point: 303.9°C at 760 mmHg
• Flash Point: 137.6°C
• Appearance: /
• Density: 1.626g/cm³
• Vapor Pressure: 0.00163mmHg at 25°C
• Refractive Index: 1.639
• CAS DataBase Reference: 1-IODO-2-PHENOXY-BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-IODO-2-PHENOXY-BENZENE(34883-46-0)
• EPA Substance Registry System: 1-IODO-2-PHENOXY-BENZENE(34883-46-0)

Safety Data

• Hazardous Substances Data: 34883-46-0(Hazardous Substances Data)

Usage

General Description

1-Iodo-2-phenoxy-benzene, also known as o-iodophenyl phenyl ether, is a chemical compound with the molecular formula C12H9IO. It is an organohalogen compound that consists of a benzene ring with an iodine atom substituted at the 1-position and a phenoxy group at the 2-position. This chemical is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also used as a precursor for the preparation of other organic compounds. 1-Iodo-2-phenoxy-benzene is a colorless to pale yellow liquid with a characteristic aromatic odor and is primarily used in research and industrial applications in the manufacture of various products. It is important to handle and store this chemical with proper safety precautions 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

• 88-73-3 2-Chloronitrobenzene 
• 71-43-2 benzene 
• 591-50-4 iodobenzene 
• 533-58-4 2-Iodophenol 
• 108-95-2 phenol 
• 1493-27-2 ortho-nitrofluorobenzene 
• 26838-86-8 pyridine-2-carboxylic acid phenyl ester 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 615-42-9 1,2-Diiodobenzene 
• 2216-12-8 1-nitro-2-phenoxy-benzene 
• 2689-07-8 2-chlorodiphenyl ether 
• 66003-76-7 Diphenyliodonium triflate 
• 96379-65-6 (cyclo-C₆H₁₁)3SnC₆H₄-o-C₆H₅ 
• 7553-56-2 iodine 

Downstream Products

• 95161-70-9 1-o-Phenoxyphenyl-naphthalin 
• 1259293-43-0 2,7-dibromo-9-(2-phenoxyphenyl)-9-fluorenol 
• 1259313-87-5 spiro(2,7-bis[4-methoxyphenyl]fluorene-9,9'-xanthene) 
• 1259313-88-6 spiro(2,7-bis[4-hydroxyphenyl]fluorene-9,9'-xanthene) 
• 1259293-47-4 C₃₉H₂₀F₈O 
• 108238-09-1 2-phenoxyphenylboronic acid 
• 3379-37-1 1,2-diphenoxybenzene 
• 1469991-11-4 4'-methyl-2-phenoxy-1,1-biphenyl 
• 100149-25-5 10-phenyldibenzo[b,f]oxepine 
• 1028267-14-2 3-(2-phenoxy-phenyl)-prop-2-yn-1-ol 
• 132-64-9 dibenzofuran 
• 3586-12-7 3-phenoxyaniline 
• 95161-71-0 2-o-Phenoxyphenyl-naphthalin 
• 101-84-8 diphenylether 

Relevant articles and documents

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

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 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.