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1,4-DIIODO-2,5-BIS(NONYLOXY)BENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

149762-44-7

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149762-44-7 Usage

Chemical Structure

1,4-DIIODO-2,5-BIS(NONYLOXY)BENZENE is a chemical compound that consists of benzene rings with two iodine atoms and two nonyl groups attached to it.

Industrial Applications

It is used in various industrial applications, such as in the manufacturing of dyes, pigments, and pharmaceuticals.

Polymer Additive

It is also used as a polymer additive.

Production of Other Chemicals

It is used in the production of various other chemicals.

Chemical Stability

1,4-DIIODO-2,5-BIS(NONYLOXY)BENZENE is known for its high chemical stability and resistance to degradation.

Industrial Processes

Due to its stability, it is a desirable choice in many industrial processes.

Environmental Impact

It is important to handle 1,4-DIIODO-2,5-BIS(NONYLOXY)BENZENE with care, as it can be toxic and harmful to the environment if released in large quantities.

Safety Precautions

Proper handling and storage procedures should be followed to prevent any potential harm to the environment or human health.

Check Digit Verification of cas no

The CAS Registry Mumber 149762-44-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,7,6 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 149762-44:
(8*1)+(7*4)+(6*9)+(5*7)+(4*6)+(3*2)+(2*4)+(1*4)=167
167 % 10 = 7
So 149762-44-7 is a valid CAS Registry Number.

149762-44-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-diiodo-2,5-di(nonoxy)benzene

1.2 Other means of identification

Product number -
Other names -

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:149762-44-7 SDS

149762-44-7Upstream product

149762-44-7Relevant academic research and scientific papers

Multitiered 2D π-stacked conjugated polymers based on pseudo-geminal disubstituted [2.2]paracyclophane

Jagtap, Subodh P.,Collard, David M.

, p. 12208 - 12209 (2010)

Interchain interactions between π-systems have a strong effect on the electronic structure of conjugated organic materials. This influence has previously been explored by the spectroscopic and electrochemical characterization of molecules in which pairs of conjugated oligomers are held in a stacked fashion by attachment to a rigid scaffold. We have prepared a new polymer which uses a pseudo-geminal disubstituted [2.2]paracyclophane scaffold to hold 1,4-bis(phenylethynyl)-2,5-dialkoxybenzene (PE3) chomophores in a π-stacked fashion over their entire length and in an extended multitier arrangement. Solutions of this new polymer display a Stokes shift of 171 nm, compared to just ca. 30 nm for previous models in which only the terminal phenyl rings of the PE3 chromophore are held in a stacked arrangement. This suggests that interchain interactions of π-systems over their entire length in a multitier assembly provides for relaxation of the excited state to a stable phane electronic state which is responsible for emission. This stabilization is not available in the stacked dimer or other regioisomers of the polymer which possess lesser degrees of overlap. Thus, the architecture of the soluble polymer mimics that of segments of conjugated polymers in semiconducting thin films and will provide a platform for the exploration of the nature of charge carriers and excitons in these important materials.

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