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CAS 1008138-66-6

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2-METHYL-5-NITRO-PYRIDINE-BORONIC ACID PINACOL ESTER

Description:
2-Methyl-5-nitro-pyridine-boronate pinacol ester is an organoboron compound characterized by the presence of a boronic acid moiety, which is typically used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. This compound features a pyridine ring substituted with a methyl group and a nitro group, which can influence its reactivity and solubility. The pinacol ester formation enhances the stability of the boronic acid, making it more suitable for various synthetic applications. Generally, boronic esters are known for their ability to participate in nucleophilic reactions, and the presence of the nitro group can introduce additional electronic effects, potentially increasing the electrophilicity of the boron center. The compound is likely to be a solid at room temperature and may exhibit moderate solubility in organic solvents. Safety data should be consulted for handling, as nitro compounds can be sensitive and may pose health risks. Overall, this compound serves as a valuable intermediate in the synthesis of more complex organic molecules.
Formula:C12H17BN2O4
Synonyms:
  • 2-METHYL-5-NITRO-PYRIDINE-BORONIC ACID PINACOL ESTER
  • Pyridine, 2-methyl-5-nitro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-methyl-5-nitro-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 2-Methyl-5-nitro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 2-Methyl-5-nitropyridine-3-boronic acid pinacol ester
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