162101-25-9
162101-25-9
Chemical Structure
2,6-Difluorophenylboronic acid
- CAS No.: 162101-25-9
- Formula:C6H5BF2O2
- Molecular Weight:157.91
IUPAC Name: (2,6-difluorophenyl)boronic acid
InChIKey: DBZAICSEFBVFHL-UHFFFAOYSA-N
SMILES: FC1=C(B(O)O)C(F)=CC=C1
Biological Activity: 2,6-Difluorophenylboronic acid is an ortho-substituted phenylboronic acid bearing two fluorine substituents at the 2- and 6-positions, and it serves as an arylboron substrate in Suzuki-Miyaura coupling reactions. 2,6-Difluorophenylboronic acid is used in organic synthesis-related research[1][2].
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2,6-Difluorophenylboronic acid | 99.74% | 2,6-Difluorophenylboronic acid is an ortho-substituted phenylboronic acid bearing two fluorine substituents at the 2- and 6-positions, and it serves as an arylboron substrate in Suzuki-Miyaura coupling reactions. 2,6-Difluorophenylboronic acid is used in organic synthesis-related research. | ||||||||||||||||||||
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References
- [1]. Georgiou I, et al. Versatile self-adapting boronic acids for H-bond recognition: from discrete to polymeric supramolecules. Journal of the American Chemical Society. 2017 Feb 22;139(7):2710-27.
- [2]. Cohen DT, et al. An Umpolung Approach for the Chemoselective Arylation of Selenocysteine in Unprotected Peptides. Journal of the American Chemical Society. 2015 Aug 12;137(31):9784-7.
