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CAS 262376-31-8

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

Description:
4,4,5,5-Tetramethyl-2-[3-(trifluoromethoxy)phenyl]-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 contains a trifluoromethoxy group, which enhances its reactivity and solubility in organic solvents. The presence of the tetramethyl substituents contributes to its steric bulk, potentially influencing its reactivity and interactions with other molecules. The trifluoromethoxy group is known for its electron-withdrawing properties, which can affect the electronic characteristics of the phenyl ring, making it a useful moiety in various chemical applications, including medicinal chemistry and materials science. Additionally, the compound's boron atom can participate in various reactions, such as Suzuki coupling, making it valuable in synthetic organic chemistry. Overall, this compound's distinctive structure and functional groups make it an interesting subject for research and application in advanced chemical synthesis.
Formula:C13H16BF3O3
InChI:InChI=1/C13H16BF3O3/c1-11(2)12(3,4)20-14(19-11)9-6-5-7-10(8-9)18-13(15,16)17/h5-8H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cccc(c2)OC(F)(F)F)O1
Synonyms:
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[3-(trifluoromethoxy)phenyl]-
  • 3-Trifluoromethoxyphenylboronic acid pinacol ester
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