4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
97%
- Product Code: 118916
CAS:
1152441-29-6
Molecular Weight: | 237.08 g./mol | Molecular Formula: | C₁₂H₁₇BFNO₂ |
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EC Number: | MDL Number: | MFCD16996293 | |
Melting Point: | Boiling Point: | 356.4±32.0°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules. It is also utilized in the preparation of bioactive compounds, including potential drug candidates targeting various diseases. Additionally, its fluorine substituent enhances its utility in the design of molecules with improved metabolic stability and binding affinity. Researchers often employ it in the development of novel materials and ligands for catalytic processes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $58.31 |
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0.250 | 10-20 days | $88.58 |
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1.000 | 10-20 days | $225.75 |
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5.000 | 10-20 days | $994.58 |
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4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules. It is also utilized in the preparation of bioactive compounds, including potential drug candidates targeting various diseases. Additionally, its fluorine substituent enhances its utility in the design of molecules with improved metabolic stability and binding affinity. Researchers often employ it in the development of novel materials and ligands for catalytic processes.
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