1,3-dibromo-5-(tert-butyl)-2-methoxybenzene
$250.00
CAS No.: 132268-08-7
Catalog No.: 193826
Purity: 95%
MF: C11H14Br2O
MW: 322.04
Storage: 2-8 degree Celsius
SMILES: BrC1=C(C(=CC(=C1)C(C)(C)C)Br)OC
Catalog No.: 193826
Purity: 95%
MF: C11H14Br2O
MW: 322.04
Storage: 2-8 degree Celsius
SMILES: BrC1=C(C(=CC(=C1)C(C)(C)C)Br)OC
For R&D use only. Not for human or animal use.
1,3-dibromo-5-(tert-butyl)-2-methoxybenzene; CAS No.: 132268-08-7;1,3-dibromo-5-(tert-butyl)-2-methoxybenzene. PROPERTIES: 1,3-dibromo-5-(tert-butyl)-2-methoxybenzene is a multiply substituted aromatic compound with molecular formula C10H13Br2O. It generally exists as a colorless to pale yellow crystalline solid with a melting point of approximately 65-68 C. The compound has low water solubility but dissolves in organic solvents like dichloromethane or THF. It exhibits moderate thermal stability but may release toxic bromine vapors when exposed to high temperatures or flames. Proper storage involves keeping it in airtight containers below 20 C, protected from light and moisture. APPLICATIONS: In organic synthesis, this compound serves as a versatile intermediate for creating highly substituted aromatic systems. The dibromo functionality enables cross-coupling reactions to form biaryl structures, while the tert-butyl group provides steric protection and the methoxy group offers electron-donating effects (Tetrahedron Letters). In pharmaceutical research, the compound contributes to the development of antimicrobial and anticancer agents where the brominated aromatic scaffold enhances binding to biological targets (European Journal of Medicinal Chemistry). Its structure makes it suitable for creating building blocks for organic electronics, where the electron-withdrawing bromine atoms modulate electronic properties of derived materials (Journal of Materials Chemistry C).
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