168267-41-2
168267-41-2
Chemical Structure
3,4-Difluorophenylboronic acid
- No. CAS: 168267-41-2
- Formula:C6H5BF2O2
- Molecular Weight:157.91
IUPAC Name: (3,4-difluorophenyl)boronic acid
InChIKey: RMGYQBHKEWWTOY-UHFFFAOYSA-N
SMILES: FC1=CC=C(B(O)O)C=C1F
Biological Activity: 3,4-Difluorophenylboronic acid is an arylboronic acid that functions as a phenylating and cross-coupling reagent in palladium-catalyzed Suzuki C-C coupling reactions. 3,4-Difluorophenylboronic acid can serve as a biomaterial or organic compound for life science-related research[1][2].
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3,4-Difluorophenylboronic acid | 99.90% | 3,4-Difluorophenylboronic acid is an arylboronic acid that functions as a phenylating and cross-coupling reagent in palladium-catalyzed Suzuki C-C coupling reactions. 3,4-Difluorophenylboronic acid can serve as a biomaterial or organic compound for life science-related research. | ||||||||||||||||||||
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References
- [1]. Tahmasbi B, et al. Magnetic MCM-41 nanoparticles as a support for the immobilization of a palladium organometallic catalyst and its application in C–C coupling reactions[J]. New Journal of Chemistry, 2019, 43(36): 14485-14501.
- [2]. Geivandov R C, Mezhnev V, Geivandova T. New Fluorine Substituted Liquid Crystal Containing Bicyclo [2.2. 2] Octane Unit[J]. Molecular Crystals and Liquid Crystals, 2011, 542(1): 106/[628]-114/[636].
