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CAS 190788-60-4

:

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

Description:
2-(2-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, with CAS number 190788-60-4, is a boron-containing organic compound characterized by its dioxaborolane structure. This compound features a boron atom coordinated to two oxygen atoms within a five-membered ring, which is further substituted with a methoxyphenyl group and four methyl groups. The presence of the methoxy group enhances its solubility in organic solvents and may influence its reactivity and interaction with other chemical species. The tetramethyl substituents contribute to the compound's steric bulk, potentially affecting its stability and reactivity in various chemical reactions, particularly in cross-coupling reactions commonly used in organic synthesis. Additionally, the dioxaborolane framework is known for its utility in the formation of boronate esters, which are valuable intermediates in organic synthesis. Overall, this compound is of interest in the fields of medicinal chemistry and materials science due to its unique structural features and potential applications.
Formula:C13H19BO3
InChI:InChI=1S/C13H19BO3/c1-12(2)13(3,4)17-14(16-12)10-8-6-7-9-11(10)15-5/h6-9H,1-5H3
InChI key:InChIKey=ASDFSWMHZSWXPO-UHFFFAOYSA-N
SMILES:O(C)C1=C(C=CC=C1)B2OC(C)(C)C(C)(C)O2
Synonyms:
  • 1,3,2-Dioxaborolane, 2-(2-methoxyphenyl)-4,4,5,5-tetramethyl-
  • 2-(2-Methoxyphenyl)-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane
  • 2-(2-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-
  • 2-Methoxybenzeneboronic Acid, Pinacol Ester
  • 2-Methoxybenzeneboronic acid, pinacol ester 97%
  • 2-Methoxyphenylboronic Acid, Pinacol Ester
  • o-(Pinacolboryl)anisole
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