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886593-45-9

(4-(2-Hydroxypropan-2-yl)phenyl)boronic acid

Catalog#: AR003KOT  |   CAS#: 886593-45-9  |   MDL#: MFCD09992905  |   MF: C9H13BO3  |   MW: 180.0087

Packsize Purity Price Availability Quantity
250mg 97% $5.00 Global Stock Buy Now Add To Cart
1g 97% $10.00 Global Stock Buy Now Add To Cart
5g 97% $40.00 Global Stock Buy Now Add To Cart
10g 97% $80.00 Global Stock Buy Now Add To Cart
25g 97% $199.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003KOT
Chemical Name (4-(2-Hydroxypropan-2-yl)phenyl)boronic acid
CAS Number 886593-45-9
Molecular Formula C9H13BO3
Molecular Weight 180.0087
MDL Number MFCD09992905
SMILES OB(c1ccc(cc1)C(O)(C)C)O

The (4-(2-Hydroxypropan-2-yl)phenyl)boronic acid is a versatile compound widely utilized in chemical synthesis as a key component for building complex organic molecules. With its boronic acid functionality, this compound serves as a crucial building block in the field of organic chemistry, particularly in the development of pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, (4-(2-Hydroxypropan-2-yl)phenyl)boronic acid acts as a valuable reagent for Suzuki-Miyaura cross-coupling reactions, a fundamental tool for forming carbon-carbon bonds. This reaction enables the coupling of an aryl or vinyl boronic acid with an organic halide or pseudohalide, leading to the creation of structurally diverse products. The versatility of this reaction makes it a staple in the construction of complex molecules found in various industries.Furthermore, the hydroxyl group present in (4-(2-Hydroxypropan-2-yl)phenyl)boronic acid offers an additional site for functionalization, allowing for further modification and customization of the molecule to tailor its properties for specific applications. Its unique structural features make it a valuable building block for synthesizing biologically active compounds, catalysts, and advanced materials that are crucial for scientific research and industrial applications.
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