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641144-16-3

(10-Bromoanthracen-9-yl)boronic acid

Catalog#: AR003EJ2  |   CAS#: 641144-16-3  |   MDL#: MFCD06411293  |   MF: C14H10BBrO2  |   MW: 300.9430

Packsize Purity Price Availability Quantity
250mg 97% $12.00 Global Stock Buy Now Add To Cart
1g 97% $30.00 Global Stock Buy Now Add To Cart
5g 97% $107.00 Global Stock Buy Now Add To Cart
10g 97% $180.00 Global Stock Buy Now Add To Cart
25g 97% $437.00 Global Stock Buy Now Add To Cart
50g 97% $769.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003EJ2
Chemical Name (10-Bromoanthracen-9-yl)boronic acid
CAS Number 641144-16-3
Molecular Formula C14H10BBrO2
Molecular Weight 300.9430
MDL Number MFCD06411293
SMILES OB(c1c2ccccc2c(c2c1cccc2)Br)O

The (10-Bromoanthracen-9-yl)boronic acid is a versatile compound widely utilized in chemical synthesis, particularly in the field of organic chemistry. Due to its unique structure and reactivity, this compound serves as a valuable building block for the creation of various complex organic molecules.One of the primary applications of (10-Bromoanthracen-9-yl)boronic acid is in cross-coupling reactions, where it acts as a key component in Suzuki-Miyaura coupling reactions. This reaction is commonly used to form carbon-carbon bonds between an aryl or vinyl boronic acid and an aryl or vinyl halide or pseudohalide. The resulting product is a biaryl or polyaryl compound, which is of great importance in the synthesis of pharmaceuticals, agrochemicals, and materials science.Additionally, (10-Bromoanthracen-9-yl)boronic acid can also participate in other types of coupling reactions, such as Heck and Sonogashira reactions, further expanding its synthetic utility. These reactions allow for the introduction of the (10-Bromoanthracen-9-yl)boronic acid moiety into various molecular frameworks, enabling the synthesis of diverse and intricate organic structures.In summary, the (10-Bromoanthracen-9-yl)boronic acid is a valuable reagent in chemical synthesis, particularly in the construction of complex organic molecules through cross-coupling reactions. Its versatility and ability to form carbon-carbon bonds make it an essential tool for organic chemists working in the field of drug discovery, materials science, and beyond.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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