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CAS 870195-94-1

:

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

Description:
2-(2-Chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane structure, which features a boron atom bonded to two oxygen atoms and a carbon atom in a cyclic arrangement. This compound contains a chlorophenyl group, contributing to its aromatic properties and potential reactivity. The presence of tetramethyl groups enhances its steric bulk, which can influence its chemical behavior and solubility. Typically, compounds like this are of interest in organic synthesis, particularly in cross-coupling reactions, due to the reactivity of the boron atom. The chlorophenyl moiety may also impart specific electronic properties, making it suitable for applications in pharmaceuticals or materials science. As with many organoboron compounds, it may exhibit unique interactions with other reagents, making it valuable in various synthetic pathways. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.
Formula:C12H16BClO2
InChI:InChI=1/C12H16BClO2/c1-11(2)12(3,4)16-13(15-11)9-7-5-6-8-10(9)14/h5-8H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccccc2Cl)O1
Synonyms:
  • 1,3,2-Dioxaborolane, 2-(2-chlorophenyl)-4,4,5,5-tetramethyl-
  • 2-Chlorophenylboronic Acid, Pinacol Ester
  • 2-(2-Chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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