Description
1,4-Di-t-butyl-2,5-bis(2-methoxyethoxy)benzene (CAS No. 1350770-63-6) is a high-purity, synthetic aromatic compound with the molecular formula C20H34O4. This derivative of benzene features two tert-butyl groups and two 2-methoxyethoxy substituents, providing unique steric and electronic properties ideal for advanced research applications. With a molecular weight of 338.48 g/mol, this compound is characterized by its exceptional stability and solubility in organic solvents, making it suitable for use in materials science, electrochemistry, and ligand design. Available in rigorously tested batches, our product ensures consistency for demanding laboratory and industrial applications.
Properties
- CAS Number: 1350770-63-6
- Complexity: 309
- IUPAC Name: 1,4-ditert-butyl-2,5-bis(2-methoxyethoxy)benzene
- InChI: InChI=1S/C20H34O4/c1-19(2,3)15-13-18(24-12-10-22-8)16(20(4,5)6)14-17(15)23-11-9-21-7/h13-14H,9-12H2,1-8H3
- InChI Key: BXGAYPHFADZNDI-UHFFFAOYSA-N
- Exact Mass: 338.24570956
- Molecular Formula: C20H34O4
- Molecular Weight: 338.5
- SMILES: CC(C)(C)C1=CC(=C(C=C1OCCOC)C(C)(C)C)OCCOC
- Topological: 36.9
- Monoisotopic Mass: 338.24570956
- Synonyms: 1350770-63-6, 1,4-Di-t-butyl-2,5-bis(2-methoxyethoxy)benzene, 1,4-Di-tert-butyl-2,5-bis(2-methoxyethoxy)benzene, MFCD30183434, 1,4-Bis(2-methoxyethoxy)-2,5-di-tert-butylbenzene, SCHEMBL9978253, BXGAYPHFADZNDI-UHFFFAOYSA-N, 2,5-di-t-butyl-1,4-bis(2-methoxyethoxy)benzene, 1,4-ditert-butyl-2,5-bis(2-methoxyethoxy)benzene, 1,4-bis(2-methoxyethoxy)-2,5-di-tert-butyl-benzene, 1,4-Di-tert-butyl-2,5-bis (2-methoxyethoxy)benzene, 99.5%, anhydrous, 1,4-Di-t-butyl-2,5-bis(2-methoxyethoxy)benzene, 99+% Redox shuttle ANL-RS2
Application
1,4-Di-t-butyl-2,5-bis(2-methoxyethoxy)benzene is widely utilized as a redox-active component in non-aqueous electrolytes for energy storage systems, including lithium-ion batteries. Its sterically hindered structure enhances electrochemical stability, making it valuable for high-voltage applications. Researchers also employ it as a building block for supramolecular chemistry and as a ligand precursor in catalytic systems. Additionally, its solubility properties make it suitable for use in organic synthesis and polymer research.
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