B-(1-Methyl-1H-indazol-4-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a 1-methyl-1H-indazole moiety. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The indazole ring contributes to its aromatic character and potential biological activity. The compound is often utilized in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. Additionally, its boronic acid functionality allows for potential applications in drug development, particularly in the design of inhibitors targeting specific enzymes or receptors. The stability and reactivity of B-(1-Methyl-1H-indazol-4-yl)boronic acid can be influenced by factors such as pH and the presence of other functional groups, making it a versatile building block in chemical research and development.

B-(1-Methyl-1H-indazol-4-yl)boronic acid

1001907-60-3: 1-Methylindazole-4-boronic acid, Boronic acid, B-(1-methyl-1H-indazol-4-yl)-, (1-Methyl-1H-indazol-4-yl)boronic acid, B-(1-Methyl-1H-indazol-4-yl)boronic acid, (1-Methylindazol-4-yl)boronic acid

1-Methyl-1H-indazole-4-boronic acid

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CAS 1001907-60-3: B-(1-Methyl-1H-indazol-4-yl)boronic acid

1-Methyl-1H-indazole-4-boronic acid

Ref: FT-M11226

1-Methylindazole-4-boronic acid

Ref: 3D-FM53520

1-Methyl-1H-indazole-4-boronic acid

Ref: 54-OR60109

Boronic acid, B-(1-methyl-1H-indazol-4-yl)-

Ref: IN-DA00016I

(1-Methyl-1H-indazol-4-yl)boronic acid

Ref: 10-F237003