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CAS 1073354-97-8

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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinamine

Description:
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinamine is a chemical compound characterized by its unique structure, which includes a pyridinamine moiety and a dioxaborolane group. The presence of the dioxaborolane ring contributes to its potential reactivity, particularly in boron chemistry, where it can participate in various reactions such as Suzuki coupling. The tetramethyl substituents enhance its steric properties, which can influence its reactivity and solubility in organic solvents. This compound is typically used in organic synthesis and may serve as a building block in the development of pharmaceuticals or agrochemicals. Its solubility characteristics and stability under different conditions are essential for its application in synthetic pathways. Additionally, the presence of the amino group in the pyridine ring can facilitate hydrogen bonding and interactions with biological targets, making it of interest in medicinal chemistry. Overall, this compound exemplifies the intersection of boron chemistry and heterocyclic compounds, showcasing its potential utility in various chemical applications.
Formula:C11H17BN2O2
InChI:InChI=1S/C11H17BN2O2/c1-10(2)11(3,4)16-12(15-10)8-6-5-7-14-9(8)13/h5-7H,1-4H3,(H2,13,14)
InChI key:InChIKey=FSJAKASJCJZKET-UHFFFAOYSA-N
SMILES:NC1=C(B2OC(C)(C)C(C)(C)O2)C=CC=N1
Synonyms:
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinamine
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
  • 2-Aminopyridine-3-boronic acid pinacol ester
  • 2-Pyridinamine, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • [3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)pyridin-2-yl]amine
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