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CAS 1032758-99-8

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

Description:
3-Chloro-5-(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 chloro group suggests potential reactivity in nucleophilic substitution reactions, while the dioxaborolane unit may facilitate various organoboron chemistry applications, such as cross-coupling reactions. This compound is likely to exhibit moderate to high polarity due to the presence of both nitrogen and chlorine atoms, which can influence its solubility in polar solvents. Additionally, the tetramethyl substitution on the dioxaborolane enhances its stability and steric hindrance, making it a useful intermediate in organic synthesis. The compound's specific reactivity and applications would depend on the functional groups present and the conditions under which it is used. Overall, this substance is of interest in medicinal chemistry and materials science, particularly in the development of pharmaceuticals and advanced materials.
Formula:C11H16BClN2O2
InChI:InChI=1S/C11H16BClN2O2/c1-10(2)11(3,4)17-12(16-10)7-5-8(13)9(14)15-6-7/h5-6H,1-4H3,(H2,14,15)
InChI key:InChIKey=HDGMGELKCLHFIL-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C=C(Cl)C(N)=NC2
Synonyms:
  • 3-Chloro-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
  • 3-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinamine
  • 3-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
  • 2-Pyridinamine, 3-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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