CAS 1073371-93-3: 2-Nitro-5-pyridineboronic acid pinacol ester

Description: 2-Nitro-5-pyridineboronic acid pinacol ester is a chemical compound characterized by its boronic acid functionality, which is known for its ability to form reversible covalent bonds with diols and other nucleophiles. This compound features a pyridine ring substituted at the 2-position with a nitro group and at the 5-position with a boronic acid moiety that is esterified with pinacol. The presence of the nitro group introduces electron-withdrawing characteristics, which can influence the reactivity and stability of the compound. The pinacol ester form enhances the solubility and stability of the boronic acid, making it more suitable for various synthetic applications, particularly in organic synthesis and medicinal chemistry. This compound can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is valuable in the formation of carbon-carbon bonds. Additionally, its unique structural features may contribute to its potential applications in drug development and materials science. Overall, 2-Nitro-5-pyridineboronic acid pinacol ester is a versatile compound with significant utility in chemical research and synthesis.

2-NITRO-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PYRIDINE

CAS: 1073371-93-3

• Formula: C₁₁H₁₅BN₂O₄
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 250.0588

2-Nitropyridine-5-boronic acid, pinacol ester

CAS: 1073371-93-3

• Formula: C₁₁H₁₅BN₂O₄
• Purity: 98%
• Color and Shape: yellow solid
• Molecular weight: 250.06g/mol

2-Nitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

CAS: 1073371-93-3

• Purity: 95.0%
• Color and Shape: Liquid, No data available.
• Molecular weight: 250.05999755859375

2-Nitropyridine-5-boronic acid pinacol ester

CAS: 1073371-93-3

Versatile small molecule scaffold

• Formula: C₁₁H₁₅BN₂O₄
• Purity: Min. 95%
• Molecular weight: 250.06 g/mol