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663954-31-2

2-P-terphenylboronic acid

Catalog#: AR003ILY  |   CAS#: 663954-31-2  |   MDL#: MFCD08669638  |   MF: C18H15BO2  |   MW: 274.1215

Packsize Purity Price Availability Quantity
100mg 96% $9.00 Global Stock Buy Now Add To Cart
250mg 96% $15.00 Global Stock Buy Now Add To Cart
1g 96% $38.00 Global Stock Buy Now Add To Cart
5g 96% $122.00 Global Stock Buy Now Add To Cart
10g 96% $232.00 Global Stock Buy Now Add To Cart
25g 96% $390.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003ILY
Chemical Name 2-P-terphenylboronic acid
CAS Number 663954-31-2
Molecular Formula C18H15BO2
Molecular Weight 274.1215
MDL Number MFCD08669638
SMILES OB(c1ccccc1c1ccc(cc1)c1ccccc1)O

2-P-terphenylboronic acid is a versatile compound widely used in chemical synthesis, specifically in the field of organic chemistry. It serves as a valuable building block in the creation of various organic molecules and complex structures due to its unique structure and reactivity. One of the primary applications of 2-P-terphenylboronic acid is in the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. This reaction involves the coupling of an aryl boronic acid with an aryl halide in the presence of a palladium catalyst, leading to the formation of a new carbon-carbon bond. 2-P-terphenylboronic acid is a commonly used boronic acid reagent in such cross-coupling reactions, allowing for the synthesis of a wide range of biaryl compounds, which are important building blocks in the pharmaceutical and materials science industries.Furthermore, 2-P-terphenylboronic acid can also be employed in the functionalization of organic molecules through boron-oxygen bond formation. Its boronic acid functionality allows for the selective introduction of boron-containing groups into organic molecules, enabling the synthesis of diverse boron-containing compounds for various applications in medicinal chemistry, materials science, and catalysis.Overall, 2-P-terphenylboronic acid is a valuable reagent in chemical synthesis, offering chemists a powerful tool for the construction of complex organic molecules and functionalized structures through carbon-carbon bond formation and selective functionalization strategies.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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