2-amino-6-(trifluoromethyl)benzonitrile

2-amino-6-(trifluoromethyl)benzonitrile

2-bromo-1,5-dichloro-3-fluorobenzene

2-bromo-1,5-dichloro-3-fluorobenzene

2-bromo-1,3-bis(bromomethyl)benzene

$250.00
CAS No.: 25006-88-6
Catalog No.: WLZ1622
Purity: 95%
MF: C8H7Br3
MW: 342.856
Storage: 2-8 degree Celsius
SMILES: BrC1=C(C=CC=C1CBr)CBr
For R&D use only. Not for human or animal use.
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CAS NO.: 25006-88-6; 2-bromo-1,3-bis(bromomethyl)benzene. PROPERTIES: This highly brominated aromatic compound features a bromine atom and two bromomethyl groups on a benzene ring, creating a molecule with potential applications in organic synthesis and materials science. The 2-bromo-1,3-bis(bromomethyl)benzene typically appears as a white crystalline powder with limited aqueous solubility but good solubility in common organic solvents. Its molecular structure includes multiple bromine atoms that render the molecule highly reactive toward nucleophilic substitution reactions. 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-bromo-1,3-bis(bromomethyl)benzene serves as a valuable intermediate in the synthesis of highly brominated compounds and materials with specific electronic properties. The bromomethyl groups provide handles for further functionalization through nucleophilic substitution reactions. In materials science, this compound functions as a building block for creating polymers and small molecules with applications in organic electronics and optoelectronics. Additionally, the molecule finds utility in chemical biology studies where its unique electronic properties can be harnessed for developing novel imaging agents and sensors. Researchers utilizing this compound benefit from its defined substitution pattern, enabling the development of advanced materials with tailored electronic and optical characteristics.

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