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685514-61-8

(2,3-Dihydrobenzofuran-7-yl)boronic acid

Catalog#: AR006JGF  |   CAS#: 685514-61-8  |   MDL#: MFCD06801700  |   MF: C8H9BO3  |   MW: 163.9663

Packsize Purity Price Availability Quantity
100mg 97% $8.00 Global Stock Buy Now Add To Cart
250mg 97% $11.00 Global Stock Buy Now Add To Cart
500mg 97% $20.00 Global Stock Buy Now Add To Cart
1g 97% $26.00 Global Stock Buy Now Add To Cart
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Catalog Number AR006JGF
Chemical Name (2,3-Dihydrobenzofuran-7-yl)boronic acid
CAS Number 685514-61-8
Molecular Formula C8H9BO3
Molecular Weight 163.9663
MDL Number MFCD06801700
SMILES OB(c1cccc2c1OCC2)O

The (2,3-Dihydrobenzofuran-7-yl)boronic acid is a crucial reagent in chemical synthesis, particularly in the field of organic chemistry. This compound is widely used in various synthetic transformations due to its versatility and reactivity. In organic synthesis, (2,3-Dihydrobenzofuran-7-yl)boronic acid serves as a key building block for the construction of complex molecules, such as pharmaceuticals, agrochemicals, and materials.One of the primary applications of (2,3-Dihydrobenzofuran-7-yl)boronic acid is in Suzuki-Miyaura cross-coupling reactions. This palladium-catalyzed coupling reaction allows for the formation of carbon-carbon bonds between an aryl or vinyl boronic acid and an organic halide or pseudohalide. By utilizing (2,3-Dihydrobenzofuran-7-yl)boronic acid as a boronic acid partner in this reaction, chemists can introduce the (2,3-Dihydrobenzofuran-7-yl) group into a target molecule selectively and efficiently.Additionally, (2,3-Dihydrobenzofuran-7-yl)boronic acid can participate in other types of organic transformations, such as palladium-catalyzed borylation reactions, Heck couplings, and C-H activation reactions. Its ability to serve as a synthetically valuable intermediate in these reactions makes it a valuable tool for chemists looking to access novel molecular structures and compounds.Overall, the application of (2,3-Dihydrobenzofuran-7-yl)boronic acid in chemical synthesis offers a powerful strategy for the construction of complex molecules and the diversification of chemical libraries for various applications in the fields of pharmaceuticals, materials science, and agrochemicals.
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