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636987-06-9

Boronic acid, B-[4-(dimethylamino)-1-naphthalenyl]-

Catalog#: AR01R5ZO  |   CAS#: 636987-06-9  |   MDL#:  |   MF: C12H14BNO2  |   MW: 215.0561

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 AR01R5ZO
Chemical Name Boronic acid, B-[4-(dimethylamino)-1-naphthalenyl]-
CAS Number 636987-06-9
Molecular Formula C12H14BNO2
Molecular Weight 215.0561
SMILES OB(c1ccc(c2c1cccc2)N(C)C)O

B-[4-(Dimethylamino)-1-naphthalenyl]boronic acid, commonly known as $name$, is a versatile compound widely used in chemical synthesis. In organic chemistry, it serves as a valuable building block for the preparation of a variety of functional molecules. Due to its unique structure, $name$ is often employed as a key intermediate in the formation of complex organic compounds.One of the main applications of B-[4-(Dimethylamino)-1-naphthalenyl]boronic acid is in Suzuki-Miyaura cross-coupling reactions. This process involves the coupling of an arylboronic acid with an organic halide or pseudohalide in the presence of a palladium catalyst to form biaryl compounds. $name$ has been found to be a particularly effective reagent in these reactions, enabling the synthesis of a wide range of biaryl derivatives with high efficiency and selectivity.Additionally, $name$ can be utilized in the construction of heterocyclic compounds, which are essential building blocks in the pharmaceutical and materials chemistry industries. By incorporating B-[4-(Dimethylamino)-1-naphthalenyl]boronic acid into the synthetic pathway, chemists can access novel structures and functional groups that are not easily accessible through conventional methods.Overall, the unique properties of B-[4-(Dimethylamino)-1-naphthalenyl]boronic acid make it a valuable tool in chemical synthesis, enabling the efficient construction of diverse organic molecules with potential applications in drug discovery, materials science, and beyond.
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