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CAS 741709-56-8

:

ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2-carboxylate

Description:
Ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2-carboxylate is a chemical compound characterized by its unique structure, which includes a pyridine ring and a dioxaborolane moiety. The presence of the ethyl ester group contributes to its solubility in organic solvents, making it suitable for various synthetic applications. This compound is notable for its potential use in organic synthesis, particularly in cross-coupling reactions, due to the boron atom that can participate in nucleophilic substitutions. The tetramethyl groups enhance the stability of the dioxaborolane, making it less prone to hydrolysis, which is advantageous in maintaining reactivity under certain conditions. Additionally, the pyridine ring can engage in coordination chemistry, allowing for interactions with metal catalysts. Overall, this compound exemplifies the integration of boron chemistry with heterocyclic compounds, offering versatility in chemical reactivity and applications in materials science and medicinal chemistry.
Formula:C14H20BNO4
InChI:InChI=1/C14H20BNO4/c1-6-18-12(17)11-9-10(7-8-16-11)15-19-13(2,3)14(4,5)20-15/h7-9H,6H2,1-5H3
SMILES:CCOC(=O)c1cc(ccn1)B1OC(C)(C)C(C)(C)O1
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