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501944-42-9

5-Fluorobenzothiophene-2-Boronic Acid

Catalog#: AR00DIRD  |   CAS#: 501944-42-9  |   MDL#: MFCD09952068  |   MF: C8H6BFO2S  |   MW: 196.0064

Packsize Purity Price Availability Quantity
50mg 95% $281.00 2-3 weeks Buy Now Add To Cart
100mg 95% $406.00 2-3 weeks Buy Now Add To Cart
250mg 95% $570.00 2-3 weeks Buy Now Add To Cart
500mg 95% $883.00 2-3 weeks Buy Now Add To Cart
1g 95% $1,125.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $2,181.00 2-3 weeks Buy Now Add To Cart
5g 95% $3,213.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR00DIRD
Chemical Name 5-Fluorobenzothiophene-2-Boronic Acid
CAS Number 501944-42-9
Molecular Formula C8H6BFO2S
Molecular Weight 196.0064
MDL Number MFCD09952068
SMILES Fc1ccc2c(c1)cc(s2)B(O)O

5-Fluorobenzo[b]thien-2-ylboronic acid is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. As a boronic acid derivative, it serves as a valuable building block in organic chemistry, particularly in the field of Suzuki-Miyaura cross-coupling reactions. This compound is often employed as a key reagent for the introduction of the 5-Fluorobenzo[b]thien-2-yl moiety into various organic molecules, enabling the selective functionalization of aromatic systems. Its ability to participate in palladium-catalyzed coupling reactions makes it a valuable tool for the synthesis of pharmaceuticals, agrochemicals, and materials with specific structural requirements.Furthermore, the presence of the fluorine atom and the benzo[b]thiophene ring in the molecule imparts distinct electronic and steric effects, allowing for precise control over regioselectivity and enhancing the overall efficiency of the synthetic processes. Overall, 5-Fluorobenzo[b]thien-2-ylboronic acid plays a crucial role in modern organic synthesis, facilitating the construction of complex molecules with strategic synthetic importance.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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