CAS 1189746-27-7: 2-Methylindazole-5-boronic acid pinacol ester

Description: 2-Methylindazole-5-boronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and an indazole ring structure. This compound typically exhibits properties associated with boron-containing compounds, such as the ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in Suzuki coupling reactions for the synthesis of biaryl compounds. The pinacol ester moiety enhances its stability and solubility in organic solvents. Additionally, the methyl group at the 2-position of the indazole ring can influence its electronic properties and reactivity. This compound is of interest in medicinal chemistry and materials science due to its potential applications in drug development and organic synthesis. Its unique structural features contribute to its utility in various chemical transformations, making it a valuable building block in synthetic organic chemistry. As with many boronic acids and their derivatives, care should be taken in handling due to their reactivity and potential environmental impact.

2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole

CAS: 1189746-27-7

• Formula: C₁₄H₁₉BN₂O₂
• Purity: 97%
• Color and Shape: Solid
• Molecular weight: 258.1239

2-Methyl-2H-indazole-5-boronic acid, pinacol ester

CAS: 1189746-27-7

• Color and Shape: Solid
• Molecular weight: 258.12g/mol

2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole

CAS: 1189746-27-7

• Purity: 96.0%
• Color and Shape: Solid
• Molecular weight: 258.1300048828125

2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole

CAS: 1189746-27-7

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• Formula: C₁₄H₁₉BN₂O₂
• Purity: Min. 95%
• Molecular weight: 258.12 g/mol