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CAS 356570-52-0

:

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

Description:
4,4,5,5-Tetramethyl-2-(4-methylbenzyl)-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane ring structure, which features two boron atoms and a five-membered cyclic arrangement. This compound typically exhibits a high degree of stability due to the presence of the boron-oxygen bonds, which can participate in various chemical reactions, including nucleophilic substitutions and cross-coupling reactions. The presence of bulky tetramethyl groups enhances its steric hindrance, potentially influencing its reactivity and solubility in organic solvents. Additionally, the 4-methylbenzyl substituent contributes to its hydrophobic characteristics and may affect its interactions with other molecules. This compound is often utilized in organic synthesis, particularly in the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals and agrochemicals. Its specific properties, such as melting point, boiling point, and solubility, would depend on the conditions and purity of the sample. Overall, 4,4,5,5-tetramethyl-2-(4-methylbenzyl)-1,3,2-dioxaborolane is a versatile building block in synthetic organic chemistry.
Formula:C14H21BO2
InChI:InChI=1/C14H21BO2/c1-11-6-8-12(9-7-11)10-15-16-13(2,3)14(4,5)17-15/h6-9H,10H2,1-5H3
SMILES:Cc1ccc(cc1)CB1OC(C)(C)C(C)(C)O1
Synonyms:
  • 4-Methylbenzylboronic acid pinacol ester
  • 4,4,5,5-tetramethyl-2-[(4-methylphenyl)methyl]-1,3,2-dioxaborolane
  • 4-METHYLBENZYLBORONIC ACID PINACOL ESTER（WS200620）
  • 4,4,5,5-Tetramethyl-2-(4-methylbenzyl)
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetraMethyl-2-[(4-Methylphenyl)Methyl]-
  • 4-Methylbenzylboronic acid pinacol ester 97%
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