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874459-69-5

(3-(N-(tert-Butyl)sulfamoyl)-4-methoxyphenyl)boronic acid

Catalog#: AR01DE7I  |   CAS#: 874459-69-5  |   MDL#: MFCD28400500  |   MF: C11H18BNO5S  |   MW: 287.1403

Packsize Purity Price Availability Quantity
250mg 95% $174.00 Global Stock Buy Now Add To Cart
1g 95% $433.00 Global Stock Buy Now Add To Cart
5g 95% $1,299.00 Global Stock Buy Now Add To Cart
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Catalog Number AR01DE7I
Chemical Name (3-(N-(tert-Butyl)sulfamoyl)-4-methoxyphenyl)boronic acid
CAS Number 874459-69-5
Molecular Formula C11H18BNO5S
Molecular Weight 287.1403
MDL Number MFCD28400500
SMILES COc1ccc(cc1S(=O)(=O)NC(C)(C)C)B(O)O

The (3-(N-(tert-butyl)sulfaMoyl)-4-Methoxyphenyl)boronic acid is a versatile compound widely utilized in chemical synthesis as a key building block. This compound plays a crucial role in Suzuki-Miyaura cross-coupling reactions, a powerful tool in modern organic chemistry for forming carbon-carbon bonds. By serving as a boronic acid derivative, this compound can effectively participate in this palladium-catalyzed coupling reaction to create structurally complex molecules with high efficiency and selectivity.Additionally, the (3-(N-(tert-butyl)sulfaMoyl)-4-Methoxyphenyl)boronic acid is known for its ability to introduce the sulfonyl group into organic molecules during the synthetic process. This functional group can impart specific properties to the target molecules, such as enhanced stability, reactivity, or binding affinity. As a result, this compound enables chemists to tailor the properties of their synthesized compounds for various applications in medicinal chemistry, materials science, and agrochemical research.Overall, the (3-(N-(tert-butyl)sulfaMoyl)-4-Methoxyphenyl)boronic acid stands as a valuable tool in the hands of synthetic chemists, providing a strategic entry point for accessing diverse chemical space and enabling the efficient construction of intricate molecular architectures.
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GHS Pictogram N/A
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