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22362-86-3

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22362-86-3 Usage

General Description

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. 9-Iodoanthracene is primarily used as a building block in the synthesis of various organic compounds, particularly in the field of organic and medicinal chemistry. It is also used as a starting material for the production of dyes, pigments, and pharmaceuticals. Additionally, it has been studied for its potential applications in organic light-emitting diodes (OLEDs) and other optoelectronic devices due to its enhanced electronic properties. 9-Iodoanthracene is considered to be a hazardous chemical and should be handled and used with proper precautions.

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 articles and documents

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

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