156545-07-2
156545-07-2
Chemical Structure
3,5-Difluorophenylboronic acid
- CAS No.: 156545-07-2
- Formula:C6H5BF2O2
- Molecular Weight:157.91
IUPAC Name: (3,5-difluorophenyl)boronic acid
InChIKey: QWQBQRYFWNIDOC-UHFFFAOYSA-N
SMILES: FC1=CC(F)=CC(B(O)O)=C1
Biological Activity: 3,5-Difluorophenylboronic acid is a fluorinated arylboronic acid compound. As an important intermediate, 3,5-difluorophenylboronic acid can be used in the synthesis of other active compounds[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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3,5-Difluorophenylboronic acid | 99.91% | 3,5-Difluorophenylboronic acid is a fluorinated arylboronic acid compound. As an important intermediate, 3,5-difluorophenylboronic acid can be used in the synthesis of other active compounds. | ||||||||||||||||||||
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2,4-Difluorophenylboronic acid | 99.93% | 2,4-Difluorophenylboronic acid is an intermediate. 2,4-Difluorophenylboronic acid can be used to synthesize dual FGFR and VEGFR inhibitors. 2,4-Difluorophenylboronic acid can be used in the research of angiogenesis and cancer. | ||||||||||||||||||||
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2,5-Difluorophenylboronic acid | 99.72% | 2,5-Difluorophenylboronic acid is a phenylboronic acid substituted with 2,5-difluorine groups. 2,5-Difluorophenylboronic acid serves as an organic synthesis intermediate belonging to the fluorinated phenylboronic acid class. | ||||||||||||||||||||
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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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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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3,4,5-Trifluorophenylboronic acid | 99.90% | 3,4,5-Trifluorophenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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3,5-Dichlorophenylboronic acid | 3,5-Dichlorophenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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4-Chloro-3-fluorophenylboronic acid | 4-Chloro-3-fluorophenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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4-Fluoro-2-methylphenylboronic acid | 99.16% | 4-Fluoro-2-methylphenylboronic acid is an arylboronic acid. 4-Fluoro-2-methylphenylboronic acid can be used in synthesis of piperidone when reacting with 3,4-dihydropyridine-1(2H)-carboxylate. | ||||||||||||||||||||
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3-Chloro-4-fluorophenylboronic acid | 3-Chloro-4-fluorophenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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4-Fluorobenzeneboronic acid | 99.88% | 4-Fluorobenzeneboronic acid (P-Fluorophenylboronic acid) is a fluorinated arylboronic acid coupling ligand and precursor. Under the catalysis of heterogeneous palladium nanoparticles, 4-Fluorobenzeneboronic acid participates in the Suzuki-Miyaura C-C coupling reaction to generate fluorinated biphenyl derivatives. 4-Fluorobenzeneboronic acid also participates in the copper-catalyzed three-component reaction with nitrobenzene and potassium metabisulfite as substrates, and finally produces sulfonamides through the formation of arylsulfinate intermediates, copper-assisted S-N bond construction and reduction steps. | ||||||||||||||||||||
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