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CAS 374537-96-9

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2-[3-(1-Methylethyl)phenyl]-1,3,2-dioxaborolane

Description:
2-[3-(1-Methylethyl)phenyl]-1,3,2-dioxaborolane is an organoboron compound characterized by the presence of a dioxaborolane ring, which consists of a boron atom bonded to two oxygen atoms and a carbon atom in a cyclic structure. This compound features a phenyl group substituted with an isopropyl group, contributing to its hydrophobic nature and potential applications in organic synthesis and materials science. The dioxaborolane moiety is known for its ability to participate in various chemical reactions, including Suzuki coupling, making it valuable in the synthesis of complex organic molecules. Additionally, the presence of the isopropyl group can influence the compound's solubility and reactivity. Overall, this substance exhibits characteristics typical of organoboron compounds, such as moderate stability, potential for functionalization, and utility in cross-coupling reactions, which are essential in the development of pharmaceuticals and agrochemicals. Its unique structure and functional groups make it a subject of interest in both academic and industrial research.
Formula:C11H15BO2
InChI:InChI=1S/C11H15BO2/c1-9(2)10-4-3-5-11(8-10)12-13-6-7-14-12/h3-5,8-9H,6-7H2,1-2H3
InChI key:InChIKey=PLCPWJGXPKHMSG-UHFFFAOYSA-N
SMILES:C(C)(C)C=1C=C(C=CC1)B2OCCO2
Synonyms:
  • 1,3,2-Dioxaborolane, 2-[3-(1-methylethyl)phenyl]-
  • 2-(3-Isopropylphenyl)-1,3,2-dioxaborolane
  • 2-(3-Propan-2-ylphenyl)-1,3,2-dioxaborolane
  • 2-[3-(1-Methylethyl)Phenyl]-1,3,2-Dioxaborolane
  • 2-[3-(Propan-2-yl)phenyl]-1,3,2-dioxaborolane
  • 3-Cumylboronic acid ethylene glycol cyclic ester~[2-(3-Isopropyl)phenyl]-1,3,2-dioxaborolane
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