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CAS 2096339-55-6

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

Description:
5-Chloro-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 pyridine ring substituted with a chloro group and a boron-containing moiety. The presence of the tetramethyl-1,3,2-dioxaborolane group suggests that this compound may exhibit properties relevant to organoboron chemistry, such as potential applications in cross-coupling reactions or as a reagent in organic synthesis. The chloro substituent can enhance the reactivity of the pyridine ring, making it a useful intermediate in the synthesis of various pharmaceuticals or agrochemicals. Additionally, the compound's boron component may contribute to its solubility and stability in different solvents. Overall, this compound's characteristics make it a valuable candidate for further research in synthetic organic chemistry and materials science, particularly in the development of new methodologies for carbon-carbon bond formation.
Formula:C11H16BClN2O2
InChI:InChI=1S/C11H16BClN2O2/c1-10(2)11(3,4)17-12(16-10)8-5-7(13)6-15-9(8)14/h5-6H,1-4H3,(H2,14,15)
InChI key:InChIKey=JUICCTPQHBAILE-UHFFFAOYSA-N
SMILES:NC1=C(B2OC(C)(C)C(C)(C)O2)C=C(Cl)C=N1
Synonyms:
  • 5-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinamine
  • 2-Pyridinamine, 5-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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