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552331-15-4

1-(5-Bromo-2-fluorophenyl)ethanol

Catalog#: AR00DIK8  |   CAS#: 552331-15-4  |   MDL#: MFCD12406116  |   MF: C8H8BrFO  |   MW: 219.0509

Packsize Purity Price Availability Quantity
100mg 96% $9.00 Global Stock Buy Now Add To Cart
250mg 96% $15.00 Global Stock Buy Now Add To Cart
1g 96% $29.00 Global Stock Buy Now Add To Cart
5g 96% $88.00 Global Stock Buy Now Add To Cart
10g 96% $140.00 Global Stock Buy Now Add To Cart
25g 96% $280.00 Global Stock Buy Now Add To Cart
100g 96% $628.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DIK8
Chemical Name 1-(5-Bromo-2-fluorophenyl)ethanol
CAS Number 552331-15-4
Molecular Formula C8H8BrFO
Molecular Weight 219.0509
MDL Number MFCD12406116
SMILES Brc1ccc(c(c1)C(O)C)F

1-(5-Bromo-2-fluorophenyl)ethanol is a versatile compound commonly used in chemical synthesis as a valuable building block for the creation of various pharmaceuticals, agrochemicals, and fine chemicals. With its unique structure combining a bromine atom and a fluorine atom on a phenyl ring connected to an ethanol functional group, this compound offers a wide range of reactivity and applications in organic synthesis.In chemical synthesis, 1-(5-Bromo-2-fluorophenyl)ethanol serves as a key intermediate in the preparation of complex molecules. Its functional groups can undergo various transformations such as substitution, reduction, and oxidation reactions to introduce new functionalities or modify existing ones. This compound is particularly useful in the synthesis of bioactive molecules due to its ability to participate in diverse chemical reactions and form stable intermediates.Moreover, the presence of both bromine and fluorine atoms in 1-(5-Bromo-2-fluorophenyl)ethanol enhances its utility as a precursor for creating fluorinated or brominated compounds with specific properties. These modified derivatives can exhibit improved biological activities, enhanced stability, or unique physical and chemical characteristics compared to their non-fluorinated or non-brominated counterparts.Overall, the strategic incorporation of 1-(5-Bromo-2-fluorophenyl)ethanol into chemical synthesis pathways allows chemists to access a wide array of functionalized molecules with diverse applications in pharmaceutical, agricultural, and other industries.
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