4-bromo-3-cyanobenzyl bromide
$300.00
CAS No.: 1032822-10-8
Catalog No.: WLZ1746
Purity: 95%
MF: C8H5Br2N
MW: 274.943
Storage: 2-8 degree Celsius
SMILES: BrC1=C(C=C(CBr)C=C1)C#N
Catalog No.: WLZ1746
Purity: 95%
MF: C8H5Br2N
MW: 274.943
Storage: 2-8 degree Celsius
SMILES: BrC1=C(C=C(CBr)C=C1)C#N
CAS NO.: 1032822-10-8; 4-bromo-3-cyanobenzyl bromide. PROPERTIES: This highly brominated aromatic compound features a bromine atom, a cyano group, and a benzyl bromide group on a benzene ring, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 4-bromo-3-cyanobenzyl bromide typically appears as a white to off-white crystalline solid with moderate solubility in common organic solvents. Its molecular structure includes multiple bromine atoms and a cyano group that influence the electronic properties of the aromatic system. For optimal stability and to prevent premature reactions, this compound should be stored at 2-8 degree Celsius in an amber glass bottle under an inert atmosphere. When handling, appropriate safety measures including nitrile gloves and safety goggles are recommended. This compound is sensitive to light and moisture, requiring careful environmental control during storage and use. In case of skin contact, wash thoroughly with soap and water; if eye contact occurs, rinse immediately and seek medical evaluation. APPLICATIONS: The 4-bromo-3-cyanobenzyl bromide serves as a versatile building block in organic synthesis, particularly for creating alkylated bioactive molecules. The benzyl bromide group 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 cyano and bromine substituents 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.
Reviews
Write Your Own Review