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Home  > [5-Methyl-1-(oxan-2-yl)-1H-indazol-4-yl]boronic acid

AX29671

2022976-34-5 | [5-Methyl-1-(oxan-2-yl)-1H-indazol-4-yl]boronic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $30.00 $21.00 -   +
250mg 98% in stock $70.00 $49.00 -   +
1g 98% in stock $163.00 $115.00 -   +
10g 98% in stock $1,536.00 $1,075.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AX29671
Chemical Name: [5-Methyl-1-(oxan-2-yl)-1H-indazol-4-yl]boronic acid
CAS Number: 2022976-34-5
Molecular Formula: C13H17BN2O3
Molecular Weight: 260.0967
MDL Number: MFCD30802381
SMILES: OB(c1c(C)ccc2c1cnn2C1CCCCO1)O

 

Upstream Synthesis Route
  • The [5-Methyl-1-(oxan-2-yl)-1H-indazol-4-yl]boronic acid is a versatile compound that finds wide applications in chemical synthesis. This unique boronic acid derivative serves as a valuable building block in organic chemistry, particularly in the formation of complex organic molecules.In chemical synthesis, this compound is commonly used as a key reagent in Suzuki-Miyaura cross-coupling reactions. Through this reaction, the boronic acid functionality enables the selective formation of carbon-carbon bonds, allowing for the efficient assembly of structurally diverse compounds. Additionally, the [5-Methyl-1-(oxan-2-yl)-1H-indazol-4-yl]boronic acid can participate in other coupling reactions, such as Buchwald-Hartwig amination, enabling the introduction of nitrogen-containing groups into target molecules.Furthermore, the presence of the oxan-2-yl moiety in this compound adds an additional level of functionality, potentially enabling further derivatization to tailor the reactivity or properties of the final product. Overall, the [5-Methyl-1-(oxan-2-yl)-1H-indazol-4-yl]boronic acid serves as a valuable tool for chemists seeking to synthesize complex and diverse organic molecules efficiently and selectively.
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