144025-03-6
144025-03-6
Chemical Structure
2,4-Difluorophenylboronic acid
- CAS No.: 144025-03-6
- Formula:C6H5BF2O2
- Molecular Weight:157.91
IUPAC Name: (2,4-difluorophenyl)boronic acid
InChIKey: QQLRSCZSKQTFGY-UHFFFAOYSA-N
SMILES: FC1=CC=C(B(O)O)C(F)=C1
Biological Activity: 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[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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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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3,5-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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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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5-Fluoro-2-methoxyphenylboronic acid | 99.84% | 5-Fluoro-2-methoxyphenylboronic 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-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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2-Fluorophenylboronic acid | 99.99% | 2-Fluorophenylboronic acid is an organic synthesis intermediate belonging to the fluorinated arylboronic acid class. The electron-withdrawing fluorine substituent in 2-Fluorophenylboronic acid reduces its pKa, thereby enhancing boronate bond formation with diols. 2-Fluorophenylboronic acid serves as a key synthetic intermediate for inhibitors of Plasmodium phosphatidylinositol 4-kinase IIIβ (PI4K). 2-Fluorophenylboronic acid can also be used to functionalize linear polyglycerols for constructing dual dynamic covalent cross-linked hydrogels that support 3D tumor spheroid culture of various cancer cells. 2-Fluorophenylboronic acid is applicable to research related to malaria and tumors. | ||||||||||||||||||||
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4-Chloro-2-fluorobenzeneboronic acid | 99.68% | 4-Chloro-2-fluorobenzeneboronic 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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