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693286-55-4

6-Isopropyl-2-methylbenzeneboronic acid

Catalog#: AR005OG3  |   CAS#: 693286-55-4  |   MDL#: MFCD11043436  |   MF: C10H15BO2  |   MW: 178.0359

Packsize Purity Price Availability Quantity
50mg 95% $353.00 2-3 weeks Buy Now Add To Cart
100mg 95% $514.00 2-3 weeks Buy Now Add To Cart
250mg 95% $725.00 2-3 weeks Buy Now Add To Cart
500mg 95% $1,130.00 2-3 weeks Buy Now Add To Cart
1g 95% $1,440.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $2,795.00 2-3 weeks Buy Now Add To Cart
5g 95% $4,124.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR005OG3
Chemical Name 6-Isopropyl-2-methylbenzeneboronic acid
CAS Number 693286-55-4
Molecular Formula C10H15BO2
Molecular Weight 178.0359
MDL Number MFCD11043436
SMILES CC(c1cccc(c1B(O)O)C)C

(2-Isopropyl-6-methylphenyl)boronic acid, also known as $name$, is a valuable reagent in chemical synthesis due to its versatile applications. This compound serves as a key building block in organic synthesis, particularly in the field of medicinal chemistry and materials science. In chemical synthesis, (2-Isopropyl-6-methylphenyl)boronic acid is widely used as a boronic acid derivative for Suzuki-Miyaura cross-coupling reactions. This powerful and widely-used coupling reaction involves the formation of carbon-carbon bonds under mild reaction conditions in the presence of a palladium catalyst. By utilizing (2-Isopropyl-6-methylphenyl)boronic acid as a substrate in these reactions, chemists can efficiently construct complex organic molecules with high selectivity and efficiency. Furthermore, the unique structural properties of (2-Isopropyl-6-methylphenyl)boronic acid make it a valuable reagent for the synthesis of biologically active compounds and pharmaceutical intermediates. Its functional groups can undergo various transformations to introduce specific chemical moieties into target molecules, enabling the synthesis of diverse compounds with potential therapeutic applications. Overall, the application of (2-Isopropyl-6-methylphenyl)boronic acid in chemical synthesis offers chemists a versatile and powerful tool for the efficient construction of complex organic molecules with diverse functionalities and applications.
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GHS Pictogram N/A
UN# -
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