4-bromo-2-fluorothiophenol
$300.00
CAS No.: 174414-93-8
Catalog No.: 194040
Purity: 95%
MF: C6H4BrFS
MW: 207.067
Storage: 2-8 degree Celsius
SMILES: BrC1=CC(=C(C=C1)S)F
Catalog No.: 194040
Purity: 95%
MF: C6H4BrFS
MW: 207.067
Storage: 2-8 degree Celsius
SMILES: BrC1=CC(=C(C=C1)S)F
4-bromo-2-fluorothiophenol; CAS No.: 174414-93-8; 4-bromo-2-fluorothiophenol. PROPERTIES: 4-bromo-2-fluorothiophenol is a colorless to pale yellow liquid with a molecular weight of 215.0 g/mol. It has a boiling point around 175-177 C at 760 mmHg and exhibits low water solubility while being miscible with common organic solvents such as acetone, ethyl acetate, and chloroform. The compound contains a thiophenol group, which is highly reactive and imparts distinct chemical properties. Proper storage requires keeping the compound in a tightly sealed container at temperatures below 20 C, protected from light and moisture. Safety precautions are crucial due to the presence of the thiophenol group, which can be highly toxic. Protective gloves, eye protection, and adequate ventilation are essential during handling. The compound may cause serious eye damage and skin irritation, and appropriate first aid measures should be followed in case of exposure. In case of accidental release, proper containment and cleanup procedures should be implemented. APPLICATIONS: 4-bromo-2-fluorothiophenol serves as a versatile intermediate in organic synthesis, particularly in the preparation of various pharmaceuticals and specialty chemicals. Its unique substitution pattern makes it suitable for the synthesis of biologically active molecules, including certain antifungal and antibacterial agents, as documented in medicinal chemistry literature. The bromine substituent provides a convenient handle for further functionalization, such as in cross-coupling reactions. Additionally, the compound functions as a building block for certain types of conductive materials and sensors, where the thiophenol group contributes to desired electronic properties. In materials science, it is utilized in the preparation of self-assembled monolayers and other surface-modifying agents. The fluorine substituent enhances the compound's ability to participate in specific interactions, expanding its utility in supramolecular chemistry applications, as reported in recent advances in materials science.
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