2-methyl-3,4,5,6-tetramethoxybromobenzene
$300.00
CAS No.: 73875-27-1
Catalog No.: WLZ1667
Purity: 95%
MF: C11H15BrO4
MW: 291.141
Storage: 2-8 degree Celsius
SMILES: CC1=C(C(=C(C(=C1OC)OC)OC)OC)Br
Catalog No.: WLZ1667
Purity: 95%
MF: C11H15BrO4
MW: 291.141
Storage: 2-8 degree Celsius
SMILES: CC1=C(C(=C(C(=C1OC)OC)OC)OC)Br
For R&D use only. Not for human or animal use.
CAS NO.: 73875-27-1; 2-methyl-3,4,5,6-tetramethoxybromobenzene. PROPERTIES: This highly methoxylated bromobenzene features a methyl group and four methoxy groups on a benzene ring, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 2-methyl-3,4,5,6-tetramethoxybromobenzene typically appears as a white to off-white crystalline solid with moderate solubility in common organic solvents. Its molecular structure includes multiple methoxy groups that render the aromatic system highly electron-rich. For optimal stability and to prevent degradation, this compound should be stored at 2-8 degree Celsius in a tightly sealed container under anhydrous conditions. When handling, appropriate safety measures including nitrile gloves and safety goggles are essential. This compound is sensitive to moisture and may hydrolyze in aqueous environments. In case of accidental spillage, clean the area with a damp cloth and dispose of materials according to local regulations. APPLICATIONS: The 2-methyl-3,4,5,6-tetramethoxybromobenzene serves as a versatile building block in organic synthesis, particularly for creating highly substituted aromatic compounds with specific electronic properties. The bromine substituent provides a handle for cross-coupling reactions, enabling the creation of substituted benzene derivatives with diverse biological activities. In medicinal chemistry, this compound functions as an intermediate for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The multiple methoxy groups contribute to target binding affinity and selectivity. Additionally, the molecule finds utility in materials science as a monomer for creating polymers with specific electronic and optical properties. Researchers utilizing this compound can benefit from its functional group versatility, enabling the development of diverse molecular architectures for applications ranging from drug discovery to advanced materials.
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