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70799-12-1

4-[(DIMETHYLAMINO)METHYL]PHENYLBORONIC ACID

Catalog#: AR005GJM  |   CAS#: 70799-12-1  |   MDL#: MFCD01319001  |   MF: C9H14BNO2  |   MW: 179.0240

Packsize Purity Price Availability Quantity
100mg 96% $7.00 Global Stock Buy Now Add To Cart
250mg 96% $10.00 Global Stock Buy Now Add To Cart
1g 96% $23.00 Global Stock Buy Now Add To Cart
5g 96% $71.00 Global Stock Buy Now Add To Cart
10g 96% $122.00 Global Stock Buy Now Add To Cart
25g 96% $304.00 Global Stock Buy Now Add To Cart
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Catalog Number AR005GJM
Chemical Name 4-[(DIMETHYLAMINO)METHYL]PHENYLBORONIC ACID
CAS Number 70799-12-1
Molecular Formula C9H14BNO2
Molecular Weight 179.0240
MDL Number MFCD01319001
SMILES OB(c1ccc(cc1)CN(C)C)O

4-((Dimethylamino)methyl)phenylboronic acid is a versatile organic compound that serves as a valuable building block in chemical synthesis. This compound is commonly used as a boronic acid derivative in various synthetic reactions due to its unique chemical reactivity and functional group compatibility. Its integrated dimethylamino group offers a diverse range of applications in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds.In organic chemistry, 4-((Dimethylamino)methyl)phenylboronic acid plays a crucial role as a key reagent in Suzuki-Miyaura cross-coupling reactions. This classic palladium-catalyzed coupling reaction involves the coupling of an organoboron compound, such as 4-((Dimethylamino)methyl)phenylboronic acid, with an organic halide or pseudohalide to form a new carbon-carbon bond. This synthetic strategy allows for the construction of complex molecular structures with high efficiency and selectivity.Additionally, 4-((Dimethylamino)methyl)phenylboronic acid can participate in other important transformations, such as Chan-Lam coupling, borylation reactions, and metal-catalyzed functionalization reactions. Its versatile nature makes it a valuable tool for the synthesis of pharmaceuticals, agrochemicals, materials, and various fine chemicals.Furthermore, the presence of the dimethylamino group in this compound imparts unique properties, such as enhanced solubility, reactivity, and selectivity in certain reactions. This makes 4-((Dimethylamino)methyl)phenylboronic acid a highly sought-after reagent in modern organic synthesis, where precise control over functional group compatibility and reaction conditions is essential for the success of the synthetic pathway.
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