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CAS 944401-60-9

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

Description:
4-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinamine is an organic compound characterized by its complex structure, which includes a pyridine ring substituted with a chloro group and a boron-containing moiety. The presence of the chloro group enhances its reactivity, making it useful in various chemical reactions, particularly in medicinal chemistry and organic synthesis. The tetramethyl-1,3,2-dioxaborolane unit contributes to its stability and solubility in organic solvents, facilitating its application in cross-coupling reactions, such as Suzuki coupling. This compound is typically used in the development of pharmaceuticals and agrochemicals due to its ability to act as a building block in the synthesis of more complex molecules. Its unique structural features also suggest potential applications in materials science and catalysis. As with many boron-containing compounds, it may exhibit specific reactivity patterns, including the ability to form complexes with various ligands, which can be exploited in synthetic methodologies. Safety and handling precautions should be observed due to the presence of the chloro group and the potential reactivity of the boron moiety.
Formula:C11H16BClN2O2
InChI:InChI=1S/C11H16BClN2O2/c1-10(2)11(3,4)17-12(16-10)7-6-15-9(14)5-8(7)13/h5-6H,1-4H3,(H2,14,15)
InChI key:InChIKey=UDJHTGSHJMSPRJ-UHFFFAOYSA-N
SMILES:ClC=1C(=CN=C(N)C1)B2OC(C)(C)C(C)(C)O2
Synonyms:
  • 4-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinamine
  • 2-Pyridinamine, 4-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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