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CAS 69807-93-8

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4,4,5,5-tetramethyl-2-(2,4,6-trichlorophenyl)-1,3,2-dioxaborolane

Description:
4,4,5,5-Tetramethyl-2-(2,4,6-trichlorophenyl)-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique dioxaborolane structure, which features a five-membered ring containing boron and oxygen atoms. This compound is notable for its incorporation of a highly substituted aromatic ring, specifically a 2,4,6-trichlorophenyl group, which contributes to its chemical stability and potential reactivity. The presence of multiple methyl groups enhances its steric bulk, influencing its solubility and interaction with other chemical species. Typically, compounds of this nature are of interest in organic synthesis and materials science, particularly in applications involving boron chemistry, such as in the development of pharmaceuticals or agrochemicals. The chlorinated aromatic moiety may also impart specific electronic properties, making it suitable for various chemical transformations. Safety and handling considerations are essential due to the presence of chlorine atoms, which can pose environmental and health risks. Overall, this compound exemplifies the complexity and utility of boron-containing organic molecules in modern chemistry.
Formula:C12H14BCl3O2
InChI:InChI=1S/C12H14BCl3O2/c1-11(2)12(3,4)18-13(17-11)10-8(15)5-7(14)6-9(10)16/h5-6H,1-4H3
InChI key:InChIKey=BGXCPGPJHBGRPJ-UHFFFAOYSA-N
SMILES:ClC1=C(B2OC(C)(C)C(C)(C)O2)C(Cl)=CC(Cl)=C1
Synonyms:
  • 4,4,5,5-tetramethyl-2-(2,4,6-trichlorophenyl)-1,3,2-dioxaborolane
  • 2,4,6-Trichlorophenylboronic Acid Pinacol Ester
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2,4,6-trichlorophenyl)-
  • Pinacol 2,4,6-trichlorobenzeneboronate
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