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CAS 365564-07-4

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

Description:
2-(3,5-Dimethoxyphenyl)-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 typically exhibits a stable, cyclic structure that is beneficial for various chemical reactions, particularly in organic synthesis and medicinal chemistry. The presence of the 3,5-dimethoxyphenyl group enhances its solubility and reactivity, making it useful in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in forming carbon-carbon bonds. Additionally, the tetramethyl substituents contribute to the compound's steric bulk, influencing its reactivity and selectivity in chemical transformations. The compound is generally stable under standard laboratory conditions but may require careful handling due to the reactivity of boron-containing compounds. Its applications can extend to the development of pharmaceuticals, agrochemicals, and materials science, where boron compounds play a crucial role in various synthetic pathways.
Formula:C14H21BO4
InChI:InChI=1/C14H21BO4/c1-13(2)14(3,4)19-15(18-13)10-7-11(16-5)9-12(8-10)17-6/h7-9H,1-6H3
SMILES:CC1(C)C(C)(C)OB(c2cc(cc(c2)OC)OC)O1
Synonyms:
  • 3,5-Dimethoxyphenylboronic acid pinacol ester
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