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CAS 1075719-83-3

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

Description:
2-(3-Ethylphenyl)-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 colorless to pale yellow appearance and is soluble in organic solvents, making it useful in various chemical applications. The presence of the ethylphenyl group contributes to its hydrophobic nature and can influence its reactivity and interaction with other molecules. Dioxaborolanes are known for their stability and ability to participate in cross-coupling reactions, particularly in organic synthesis and materials science. The compound may also serve as a precursor for the synthesis of more complex boron-containing compounds. Its specific properties, such as melting point, boiling point, and reactivity, can vary based on environmental conditions and the presence of other functional groups. Overall, this compound is of interest in both academic research and industrial applications, particularly in the fields of organic chemistry and medicinal chemistry.
Formula:C14H21BO2
InChI:InChI=1S/C14H21BO2/c1-6-11-8-7-9-12(10-11)15-16-13(2,3)14(4,5)17-15/h7-10H,6H2,1-5H3
InChI key:InChIKey=HGQJLAFYLXBEMB-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(CC)=CC=C2
Synonyms:
  • 2-(3-Ethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 3-Ethylphenylboronic acid pinacol ester
  • 1,3,2-Dioxaborolane, 2-(3-ethylphenyl)-4,4,5,5-tetramethyl-
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