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CAS 635305-47-4

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

Description:
2-(3-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 framework. This compound contains a chlorophenyl group, contributing to its potential reactivity and applications in organic synthesis, particularly in cross-coupling reactions. The presence of tetramethyl substituents enhances its stability and solubility in organic solvents. Typically, compounds of this nature exhibit moderate to high thermal stability and can participate in various chemical transformations, making them valuable intermediates in the synthesis of pharmaceuticals and agrochemicals. The chlorophenyl moiety may also impart specific electronic properties, influencing the compound's reactivity. Additionally, the dioxaborolane structure allows for the formation of boronate esters, which are useful in Suzuki-Miyaura coupling reactions. Overall, this compound is significant in the field of synthetic organic chemistry, particularly in the development of new materials and biologically active molecules.
Formula:C12H16BClO2
InChI:InChI=1/C12H16BClO2/c1-11(2)12(3,4)16-13(15-11)9-6-5-7-10(14)8-9/h5-8H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cccc(c2)Cl)O1
Synonyms:
  • 3-Chlorophenylboronic Acid Pinacol Ester
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