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CAS 480424-69-9

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

Description:
Phenol, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1-acetate, identified by CAS number 480424-69-9, is an organic compound that features a phenolic structure modified with a boron-containing group. This compound typically exhibits characteristics common to phenols, such as being a weak acid due to the presence of the hydroxyl (-OH) group, which can donate protons in solution. The incorporation of the dioxaborolane moiety enhances its reactivity, particularly in cross-coupling reactions, making it valuable in synthetic organic chemistry. The acetate group suggests that it can undergo hydrolysis to release acetic acid, further influencing its reactivity and solubility in various solvents. Additionally, the bulky tetramethyl substituents may impart steric hindrance, affecting the compound's reactivity and interactions with other molecules. Overall, this compound is likely to be of interest in fields such as medicinal chemistry and materials science, where boron-containing compounds are often utilized for their unique properties and reactivity profiles.
Formula:C14H19BO4
InChI:InChI=1S/C14H19BO4/c1-10(16)17-12-8-6-7-11(9-12)15-18-13(2,3)14(4,5)19-15/h6-9H,1-5H3
InChI key:InChIKey=YJDMBSCTYDVXPH-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(OC(C)=O)=CC=C2
Synonyms:
  • Phenol, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1-acetate
  • Phenol, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, acetate
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