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CAS 1073312-28-3

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

Description:
2-Chloro-3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a chemical compound characterized by its unique structure, which includes a pyridine ring substituted with chlorine and fluorine atoms, as well as a boron-containing moiety. The presence of the dioxaborolane group enhances its reactivity, particularly in cross-coupling reactions, making it valuable in synthetic organic chemistry. This compound is typically used in the development of pharmaceuticals and agrochemicals due to its ability to participate in various chemical transformations. Its physical properties, such as solubility and boiling point, can vary based on the solvent and conditions used. The compound's reactivity is influenced by the electron-withdrawing effects of the chlorine and fluorine substituents, which can affect its behavior in nucleophilic and electrophilic reactions. Safety data sheets should be consulted for handling and storage guidelines, as compounds with halogen substituents can pose specific hazards. Overall, this compound exemplifies the complexity and utility of halogenated heterocycles in modern chemistry.
Formula:C11H14BClFNO2
InChI:InChI=1S/C11H14BClFNO2/c1-10(2)11(3,4)17-12(16-10)7-5-8(14)9(13)15-6-7/h5-6H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cc(c(Cl)nc2)F)O1
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