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CAS 171364-79-7

:

2-(4-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-(4-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane structure, which features a five-membered ring containing boron and oxygen atoms. This compound typically exhibits a high degree of stability due to the presence of the boron atom, which can participate in various chemical reactions, particularly in cross-coupling reactions in organic synthesis. The methoxyphenyl group enhances its solubility in organic solvents and may influence its reactivity and interaction with other molecules. Additionally, the tetramethyl substituents contribute to steric hindrance, which can affect the compound's reactivity and selectivity in chemical transformations. This compound is often utilized in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to form stable complexes and facilitate the formation of carbon-carbon bonds. Its properties make it a valuable intermediate in various chemical processes, showcasing the versatility of boron-containing compounds in modern chemistry.
Formula:C13H19BO3
InChI:InChI=1S/C13H19BO3/c1-12(2)13(3,4)17-14(16-12)10-6-8-11(15-5)9-7-10/h6-9H,1-5H3
InChI key:InChIKey=VFIKPDSQDNROGM-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC=C(OC)C=C2
Synonyms:
  • 1,3,2-Dioxaborolane, 2-(4-methoxyphenyl)-4,4,5,5-tetramethyl-
  • 2-(4-Methoxyphenyl)-4,4,5,5-tetramethyl[1,3,2]dioxaborolane
  • 4,4,5,5-Tetramethyl-2-(4-methoxyphenyl)-1,3,2-dioxaborolane
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-methoxybenzene
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anisole
  • 4-Methoxyphenyl(pinacolato)borane
  • 4-Methoxyphenylboronicacidpinacolester
  • p-(Pinacolboryl)anisole
  • 4-Methoxyphenylboronic acid pinacol ester
  • 4-Methoxyphenylboronic acid pinacol ester
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