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CAS 635305-46-3

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2-(3-Chloro-4-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-(3-Chloro-4-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique dioxaborolane structure, which features a five-membered ring containing boron and oxygen atoms. This compound exhibits a high degree of stability due to the presence of the boron atom, which can participate in various chemical reactions, particularly in the context of organic synthesis and medicinal chemistry. The presence of the chloro and fluoro substituents on the phenyl ring enhances its reactivity and potential applications in pharmaceuticals and agrochemicals. Additionally, the tetramethyl groups contribute to the compound's steric bulk, influencing its solubility and interaction with biological systems. This compound is often utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, making it valuable in the synthesis of complex organic molecules. Its specific properties, such as melting point, boiling point, and solubility, would need to be referenced from experimental data or material safety data sheets for practical applications.
Formula:C12H15BClFO2
InChI:InChI=1S/C12H15BClFO2/c1-11(2)12(3,4)17-13(16-11)8-5-6-10(15)9(14)7-8/h5-7H,1-4H3
InChI key:InChIKey=PFRXRUVRRFJIBF-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(Cl)=C(F)C=C2
Synonyms:
  • 3-Chloro-4-fluorophenylboronic acid pinacol ester
  • 2-(3-Chloro-4-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-(3-chloro-4-fluorophenyl)-4,4,5,5-tetramethyl-
  • 3-Chloro-4-fluoro-phenylboronic acid pinacol ester
  • 2-(3-Chloro-4-fluorophenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
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