Introduction of CAS:2100-42-7 | 2-Chloro-1,4-dimethoxybenzene
2-Chloro-1,4-dimethoxybenzene (2-CDMB) is an aromatic compound belonging to the class of aromatic compounds known as phenols. It is a colorless solid that is soluble in both organic and aqueous solvents. 2-CDMB has a wide range of applications in the chemical industry, and has been studied extensively for its various properties and potential applications.
Specification of CAS:2100-42-7 | 2-Chloro-1,4-dimethoxybenzene
|
ITEMS |
SPECIFICATION |
|
Density |
1.21 |
|
Boiling Point |
247ºC (759.8513 mmHg) |
|
Flash Point |
117ºC |
|
Form |
clear liquid |
|
Color |
Colorless to Almost colorless |
|
Storage condition |
Sealed in dry,Room Temperature |
Research Application of CAS:2100-42-7 | 2-Chloro-1,4-dimethoxybenzene
Role in Lignin Peroxidase Oxidation
2Cl-1,4-DMB is involved in the oxidation process catalyzed by lignin peroxidase (LiP), forming a cation radical. This process results in the formation of compounds such as 2-chloro-1,4-benzoquinone and various dimers. Interestingly, the presence of anisyl alcohol can quench the cation radical and prevent enzyme inactivation (Teunissen et al., 1998).
Catalytic Cofactor for Oxidation Processes
In a similar context, 2Cl-1,4-DMB serves as a catalytic cofactor in the oxidation of anisyl alcohol by LiP, displaying superior performance compared to other substances like veratryl alcohol. This indicates its potential application in enzymatic and oxidative processes (Teunissen & Field, 1998).
Application in Lithium-Ion Batteries
This compound has been studied as an electrolyte additive in liquid state Al-plastic film lithium-ion batteries. It shows potential in preventing electrolyte decomposition during overcharge, indicating its significance in enhancing battery safety and performance (Yong Zhang et al., 2011).
Use in Non-Aqueous Redox Flow Batteries
Derivatives of 1,4-Dimethoxybenzene, including those related to 2Cl-1,4-DMB, are used as catholytes in non-aqueous redox flow batteries. Their modification, such as by incorporating bicyclic substitutions, enhances chemical stability and solubility, crucial for battery performance and longevity (Jingjing Zhang et al., 2017).

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