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17933-03-8

Boronic acid, B-(3-methylphenyl)-

Catalog#: AR0027MT  |   CAS#: 17933-03-8  |   MDL#: MFCD00040198  |   MF: C7H9BO2  |   MW: 135.9562

Packsize Purity Price Availability Quantity
1g 98% $4.00 Global Stock Buy Now Add To Cart
5g 98% $4.00 Global Stock Buy Now Add To Cart
10g 98% $7.00 Global Stock Buy Now Add To Cart
25g 98% $9.00 Global Stock Buy Now Add To Cart
100g 98% $35.00 Global Stock Buy Now Add To Cart
500g 98% $169.00 Global Stock Buy Now Add To Cart
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Catalog Number AR0027MT
Chemical Name Boronic acid, B-(3-methylphenyl)-
CAS Number 17933-03-8
Molecular Formula C7H9BO2
Molecular Weight 135.9562
MDL Number MFCD00040198
SMILES Cc1cccc(c1)B(O)O

3-Methylphenylboronic acid, also known as meta-tolylboronic acid, is a versatile chemical compound widely used in organic synthesis. Its unique structure and reactivity make it a valuable reagent in various chemical reactions.1. Suzuki Coupling Reaction: 3-Methylphenylboronic acid is commonly employed in Suzuki coupling reactions, a powerful method for forming carbon-carbon bonds. In this process, the boronic acid group of 3-Methylphenylboronic acid reacts with an organic halide in the presence of a palladium catalyst to generate new carbon-carbon bonds. This reaction is widely utilized in the synthesis of pharmaceuticals, agrochemicals, and materials.2. Cross-Coupling Reactions: This compound also finds application in other cross-coupling reactions such as Sonogashira coupling and Heck reaction. In Sonogashira coupling, 3-Methylphenylboronic acid can react with terminal alkynes to form conjugated enynes, while in Heck reaction, it can be utilized for the synthesis of functionalized alkenes.3. Building Block in Organic Synthesis: 3-Methylphenylboronic acid serves as a valuable building block in the preparation of various molecules due to its versatile reactivity. It can be used to introduce the meta-tolyl group into organic compounds, allowing for the modification of molecular properties and functionalities.Overall, 3-Methylphenylboronic acid plays a crucial role in modern organic synthesis as a key reagent in cross-coupling reactions and a versatile building block for the construction of complex organic molecules. Its applications extend to the synthesis of pharmaceuticals, natural products, and advanced materials, highlighting its significance in the field of organic chemistry.
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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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