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CAS 871839-91-7

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6-Isopropoxypyridine-3-boronic acid pinacol ester

Description:
6-Isopropoxypyridine-3-boronic acid pinacol ester is a chemical compound characterized by its boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and is widely used in organic synthesis, particularly in Suzuki coupling reactions. This compound features a pyridine ring substituted with an isopropoxy group at the 6-position and a pinacol ester moiety, which enhances its stability and solubility in organic solvents. The presence of the boronic acid functionality allows for the formation of complexes with various substrates, making it valuable in medicinal chemistry and materials science. Its structural attributes contribute to its reactivity and potential applications in the development of pharmaceuticals and agrochemicals. Additionally, the compound's properties, such as melting point, solubility, and reactivity, can vary based on the specific conditions under which it is used, making it essential to consider these factors in practical applications.
Formula:C14H22BNO3
InChI:InChI=1/C14H22BNO3/c1-10(2)17-12-8-7-11(9-16-12)15-18-13(3,4)14(5,6)19-15/h7-10H,1-6H3
SMILES:CC(C)Oc1ccc(cn1)B1OC(C)(C)C(C)(C)O1
Synonyms:
  • Pyridine, 2-(1-Methylethoxy)-5-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-
  • 2-Isopropoxy-5-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine
  • 2-Isopropoxypyridine-5-boronicacidpinacolester
  • 2-Isopropoxypyridine-5-boronic acid pinacol ester
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