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CAS 69807-92-7

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

Description:
2-(2,6-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, with the CAS number 69807-92-7, is a boron-containing organic compound characterized by its unique dioxaborolane structure. This compound features a boron atom bonded to two oxygen atoms in a cyclic arrangement, along with a dichlorophenyl group that enhances its chemical reactivity and potential applications. The presence of tetramethyl groups contributes to its steric bulk, influencing its solubility and reactivity in various chemical environments. Typically, compounds of this nature are utilized in organic synthesis, particularly in cross-coupling reactions, due to the boron atom's ability to participate in nucleophilic substitutions. The dichlorophenyl moiety may also impart specific electronic properties, making it suitable for applications in pharmaceuticals or agrochemicals. Overall, this compound exemplifies the versatility of boron-containing compounds in synthetic chemistry, with potential implications in material science and medicinal chemistry.
Formula:C12H15BCl2O2
InChI:InChI=1S/C12H15BCl2O2/c1-11(2)12(3,4)17-13(16-11)10-8(14)6-5-7-9(10)15/h5-7H,1-4H3
InChI key:InChIKey=WKXMSUKHFIHUEW-UHFFFAOYSA-N
SMILES:ClC1=C(C(Cl)=CC=C1)B2OC(C)(C)C(C)(C)O2
Synonyms:
  • 2-(2,6-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-(2,6-dichlorophenyl)-4,4,5,5-tetramethyl-
  • Pinacol 2,6-dichlorobenzeneboronate
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