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CAS 2121512-17-0

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2-[3,5-Dichloro-4-(phenylmethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-[3,5-Dichloro-4-(phenylmethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique dioxaborolane structure, which includes a boron atom coordinated to oxygen atoms in a cyclic arrangement. This compound features a dichlorophenyl moiety and a phenylmethoxy group, contributing to its potential applications in organic synthesis and medicinal chemistry. The presence of multiple chlorine atoms enhances its reactivity and may influence its biological activity. The tetramethyl substituents on the dioxaborolane ring provide steric hindrance, which can affect the compound's stability and reactivity. Typically, compounds of this nature are studied for their roles in cross-coupling reactions, particularly in the formation of carbon-carbon bonds, making them valuable in the development of pharmaceuticals and agrochemicals. Additionally, the specific arrangement of functional groups can lead to interesting electronic properties, which may be exploited in materials science. Overall, this compound exemplifies the intersection of organic chemistry and materials science, showcasing the versatility of boron-containing compounds in various applications.
Formula:C19H21BCl2O3
InChI:InChI=1S/C19H21BCl2O3/c1-18(2)19(3,4)25-20(24-18)14-10-15(21)17(16(22)11-14)23-12-13-8-6-5-7-9-13/h5-11H,12H2,1-4H3
InChI key:InChIKey=DZFNGYWYOQKIBD-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(Cl)=C(OCC3=CC=CC=C3)C(Cl)=C2
Synonyms:
  • 1,3,2-Dioxaborolane, 2-[3,5-dichloro-4-(phenylmethoxy)phenyl]-4,4,5,5-tetramethyl-
  • 2-[3,5-Dichloro-4-(phenylmethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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