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22191-58-8

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22191-58-8 Usage

General Description

2,6-Dibromoterephthalic acid is a chemical compound with the molecular formula C8H4Br2O4. It is a derivative of terephthalic acid, which is commonly used in the production of plastics and polyester fibers. 2,6-Dibromoterephthalic acid is specifically used in the synthesis of coordination polymers and metal-organic frameworks due to its ability to coordinate with metal ions. It has also been studied for its potential applications in organic electronics and optoelectronic devices. 2,6-Dibromoterephthalic acid is a white solid at room temperature and is considered to be relatively stable under normal conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 22191-58-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,9 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22191-58:
(7*2)+(6*2)+(5*1)+(4*9)+(3*1)+(2*5)+(1*8)=88
88 % 10 = 8
So 22191-58-8 is a valid CAS Registry Number.

22191-58-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dibromoterephthalic acid

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:22191-58-8 SDS

22191-58-8Downstream Products

22191-58-8Relevant articles and documents

Hole Transfer Processes in meta- and para-Conjugated Mixed Valence Compounds: Unforeseen Effects of Bridge Substituents and Solvent Dynamics

Sch?fer, Julian,Holzapfel, Marco,Mladenova, Boryana,Kattnig, Daniel,Krummenacher, Ivo,Braunschweig, Holger,Grampp, Günter,Lambert, Christoph

, p. 6200 - 6209 (2017)

To address the question whether donor substituents can be utilized to accelerate the hole transfer (HT) between redox sites attached in para- or in meta-positions to a central benzene bridge, we investigated three series of mixed valence compounds based o

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