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1938062-31-7

2-fluoro-6-formylphenylboronic acid

Catalog#: AR00I3Q8  |   CAS#: 1938062-31-7  |   MDL#: MFCD19981524  |   MF: C7H6BFO3  |   MW: 167.9301

Packsize Purity Price Availability Quantity
100mg 97% $4.00 Global Stock Buy Now Add To Cart
250mg 97% $8.00 Global Stock Buy Now Add To Cart
1g 97% $21.00 Global Stock Buy Now Add To Cart
5g 97% $72.00 Global Stock Buy Now Add To Cart
10g 97% $144.00 Global Stock Buy Now Add To Cart
25g 97% $359.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00I3Q8
Chemical Name 2-fluoro-6-formylphenylboronic acid
CAS Number 1938062-31-7
Molecular Formula C7H6BFO3
Molecular Weight 167.9301
MDL Number MFCD19981524
SMILES O=Cc1cccc(c1B(O)O)F

B-(2-Fluoro-6-formylphenyl)boronic acid, commonly referred to as $name$, is a versatile compound frequently employed in chemical synthesis processes. This compound serves as a crucial building block in the creation of pharmaceuticals, agricultural chemicals, and advanced materials due to its unique reactivity and functional properties.In chemical synthesis, $name$ is utilized as a key reagent in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. Through this process, $name$ facilitates the coupling of aryl halides with various boronic acids, enabling the creation of complex organic molecules with high efficiency and selectivity. Additionally, $name$ is instrumental in the synthesis of heterocycles, natural products, and other structurally diverse compounds, making it indispensable in modern organic chemistry.Moreover, the presence of the fluoro and formyl functional groups in $name$ imparts desirable properties to the resulting compounds, such as enhanced bioactivity, solubility, and fluorescent characteristics. This makes $name$ a valuable tool for chemists and researchers seeking to design novel molecules with tailored properties for a wide range of applications.Overall, the application of B-(2-Fluoro-6-formylphenyl)boronic acid in chemical synthesis offers unparalleled versatility and functionality, driving innovation and discovery in the field of organic chemistry.
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