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CAS 1310404-51-3

:

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

Description:
2-Chloro-5-nitro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a chemical compound characterized by its complex structure, which includes a pyridine ring substituted with a chlorine atom and a nitro group, as well as a boron-containing moiety. The presence of the chloro and nitro groups indicates potential reactivity, making it useful in various synthetic applications, particularly in medicinal chemistry and materials science. The boron-containing group, specifically the tetramethyl-1,3,2-dioxaborolane, suggests that this compound may participate in reactions involving boron chemistry, such as Suzuki coupling reactions, which are valuable in forming carbon-carbon bonds. The compound's solubility, stability, and reactivity can be influenced by the electronic effects of the substituents on the pyridine ring. Additionally, the presence of the nitro group may enhance the compound's polarity and influence its interaction with biological systems. Overall, this compound's unique structural features make it a candidate for further research and application in various chemical contexts.
Formula:C11H14BClN2O4
InChI:InChI=1S/C11H14BClN2O4/c1-10(2)11(3,4)19-12(18-10)8-5-7(15(16)17)6-14-9(8)13/h5-6H,1-4H3
InChI key:InChIKey=TZNILTPHZHGJEH-UHFFFAOYSA-N
SMILES:ClC1=C(C=C(N(=O)=O)C=N1)B2OC(C)(C)C(C)(C)O2
Synonyms:
  • Pyridine, 2-chloro-5-nitro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-Chloro-5-nitro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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