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CAS 480424-68-8

:

2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl acetate

Description:
2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl acetate is an organoboron compound characterized by the presence of a boron-containing dioxaborolane moiety and an acetate functional group attached to a phenyl ring. This compound typically exhibits a stable structure due to the presence of the dioxaborolane, which can enhance its reactivity in various chemical transformations, particularly in cross-coupling reactions. The tetramethyl groups contribute to steric hindrance, which can influence its reactivity and solubility in organic solvents. The acetate group provides a polar functional group that can participate in hydrogen bonding and may enhance solubility in polar solvents. This compound is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to act as a boron source in reactions such as Suzuki coupling. Its unique structural features make it a valuable intermediate in synthetic chemistry.
Formula:C14H19BO4
InChI:InChI=1/C14H19BO4/c1-10(16)17-12-9-7-6-8-11(12)15-18-13(2,3)14(4,5)19-15/h6-9H,1-5H3
SMILES:CC(=O)Oc1ccccc1B1OC(C)(C)C(C)(C)O1
Synonyms:
  • Phenol, 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, acetate
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