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501944-65-6

6-FLUOROBENZO[B]THIENE-2-BORONIC ACID

Catalog#: AR00DGI2  |   CAS#: 501944-65-6  |   MDL#: MFCD09952067  |   MF: C8H6BFO2S  |   MW: 196.0064

Packsize Purity Price Availability Quantity
250mg 95% $500.00 3-4 weeks Buy Now Add To Cart
1g 95% $800.00 3-4 weeks Buy Now Add To Cart
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Catalog Number AR00DGI2
Chemical Name 6-FLUOROBENZO[B]THIENE-2-BORONIC ACID
CAS Number 501944-65-6
Molecular Formula C8H6BFO2S
Molecular Weight 196.0064
MDL Number MFCD09952067
SMILES Fc1ccc2c(c1)sc(c2)B(O)O

(6-Fluorobenzo[b]thiophen-2-yl)boronic acid is a versatile chemical reagent commonly used in organic synthesis. It serves as a key building block in the preparation of various functional molecules and pharmaceutical compounds due to its unique structural properties.One of the notable applications of (6-Fluorobenzo[b]thiophen-2-yl)boronic acid is its use in Suzuki-Miyaura cross-coupling reactions. In this widely utilized synthetic method, the boronic acid functionality of (6-Fluorobenzo[b]thiophen-2-yl)boronic acid can undergo coupling with organic halides or triflates in the presence of a palladium catalyst. This reaction enables the formation of carbon-carbon bonds, allowing for the efficient synthesis of biaryl and heteroaryl compounds.Additionally, (6-Fluorobenzo[b]thiophen-2-yl)boronic acid can participate in other important transformations such as Buchwald-Hartwig amination, Chan-Lam coupling, and metal-catalyzed borylation reactions. These diverse reactivity profiles make it a valuable tool in the construction of complex molecular structures with high precision and efficiency.Overall, the unique reactivity and versatility of (6-Fluorobenzo[b]thiophen-2-yl)boronic acid make it an indispensable component in the toolkit of synthetic chemists for the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties.
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GHS Pictogram N/A
UN# -
Hazard Statements -
Class -
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