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Anthracene, 9-iodo-, also known as 9-Iodoanthracene, is a chemical compound with the molecular formula C14H9I. It is a yellow crystalline solid that is insoluble in water and soluble in organic solvents. Anthracene, 9-iodois known for its enhanced electronic properties and is primarily used as a building block in the synthesis of various organic compounds, particularly in the fields of organic and medicinal chemistry.

22362-86-3

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22362-86-3 Usage

Uses

Used in Organic and Medicinal Chemistry:
Anthracene, 9-iodois used as a building block for the synthesis of various organic compounds, contributing to the development of new chemical entities with potential applications in pharmaceuticals and other industries.
Used in Dye and Pigment Production:
Anthracene, 9-iodoserves as a starting material for the production of dyes and pigments, offering a wide range of color options for various applications, including textiles, plastics, and printing inks.
Used in Pharmaceutical Industry:
Anthracene, 9-iodois utilized as a starting material for the synthesis of pharmaceuticals, aiding in the development of new drugs with improved therapeutic properties.
Used in Optoelectronic Devices:
Anthracene, 9-iodohas been studied for its potential applications in organic light-emitting diodes (OLEDs) and other optoelectronic devices, leveraging its enhanced electronic properties to improve device performance and efficiency.

Check Digit Verification of cas no

The CAS Registry Mumber 22362-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,6 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22362-86:
(7*2)+(6*2)+(5*3)+(4*6)+(3*2)+(2*8)+(1*6)=93
93 % 10 = 3
So 22362-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H9I/c15-14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-9H

22362-86-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-iodoanthracene

1.2 Other means of identification

Product number -
Other names 9-iodo-anthracene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22362-86-3 SDS

22362-86-3Upstream product

22362-86-3Relevant academic research and scientific papers

Generation of electrophilic iodine from iodine monochloride in neutral media. Iodination and protodeiodination of carbazole

Filimonov,Krasnokutskaya,Lesina

, p. 875 - 880 (2007/10/03)

In reaction of iodine monochloride with CF3COOAg, CH 3COONa or (CH3COO)2Pb in acetonitrile and acetic acid the chloride is bonded by metal cations, and electrophilic iodine is generated able to easily iodinate a

Iodine Cyanide Promoted Iodination of Aromatic Compounds. A Simple Synthesis of 1-Iodopyrene

Radner, Finn

, p. 481 - 484 (2007/10/02)

A simple method for the iodination of reactive aromatic compounds, using ICN in the presence of a Lewis acid as the source of iodine, is presented. 1-Iodopyrene is obtained in 81percent isolated yield from the reaction of pyrene and ICN with AlCl3 in CH3NO2/(C2H5)2O.Anthracene undergoes partial chlorination in the presence of AlCl3, but with BF3, 9-iodoanthracene is obtained in 48percent isolated yield.

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