2-bromo-5-iodo-1,3-bis(trifluoromethyl)benzene
$250.00
CAS No.: 2383655-21-6
Catalog No.: 193911
Purity: 95%
MF: C8H2BrF6I
MW: 418.9
Storage: 2-8 degree Celsius
SMILES: BrC1=C(C=C(C=C1C(F)(F)F)I)C(F)(F)F
Catalog No.: 193911
Purity: 95%
MF: C8H2BrF6I
MW: 418.9
Storage: 2-8 degree Celsius
SMILES: BrC1=C(C=C(C=C1C(F)(F)F)I)C(F)(F)F
2-bromo-5-iodo-1,3-bis(trifluoromethyl)benzene; CAS No.: 2383655-21-6;2-bromo-5-iodo-1,3-bis(trifluoromethyl)benzene. PROPERTIES: 2-bromo-5-iodo-1,3-bis(trifluoromethyl)benzene is a brominated, iodinated, and trifluoromethylated aromatic compound with molecular formula C8H4BrF6I. It typically exists as a colorless liquid with a boiling point around 150-155 C. The compound has limited water solubility but dissolves well in organic solvents like dichloromethane or carbon tetrachloride. It exhibits moderate thermal stability but may decompose when exposed to high temperatures or strong bases, releasing toxic bromine and iodine vapors. Proper storage involves keeping it in tightly sealed containers below 25 C, away from heat sources and incompatible materials. APPLICATIONS: In organic synthesis, this compound serves as a highly versatile intermediate for creating complex aromatic systems. The bromo and iodo substituents provide multiple sites for cross-coupling reactions, enabling the formation of diverse biaryl structures (The Journal of Organic Chemistry). In pharmaceutical research, 2-bromo-5-iodo-1,3-bis(trifluoromethyl)benzene contributes to the development of radiopharmaceuticals where the iodine isotope can be incorporated for imaging or therapeutic applications (Journal of Labelled Compounds & Radiopharmaceuticals). The compound also finds application in materials science as a building block for organic electronics, where its multiple electron-withdrawing groups modulate the electronic properties of derived materials (Advanced Materials).
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