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CAS 214360-69-7

:

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

Description:
2-(2,4-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 coordinated to two oxygen atoms and a carbon atom. This compound typically exhibits a stable, cyclic structure that is useful in various organic synthesis applications, particularly in the formation of carbon-boron bonds. The presence of the dimethoxyphenyl group enhances its reactivity and solubility in organic solvents, making it suitable for use in cross-coupling reactions, such as Suzuki-Miyaura coupling. Additionally, the tetramethyl substituents contribute to the steric bulk around the boron center, influencing its reactivity and selectivity in chemical reactions. This compound is often utilized in the development of pharmaceuticals and agrochemicals, as well as in materials science for the synthesis of functionalized polymers. Its properties, including stability and reactivity, make it a valuable intermediate in synthetic organic chemistry.
Formula:C14H21BO4
InChI:InChI=1/C14H21BO4/c1-13(2)14(3,4)19-15(18-13)11-8-7-10(16-5)9-12(11)17-6/h7-9H,1-6H3
SMILES:CC1(C)C(C)(C)OB(c2ccc(cc2OC)OC)O1
Synonyms:
  • 2,4-Dimethoxyphenylboronic Acid, Pinacol Ester
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