Potassium (4-((dimethylamino)methyl)phenyl)trifluoroborate
98%
- Product Code: 130344
CAS:
1988699-55-3
| Molecular Weight: | 241.11 g./mol | Molecular Formula: | C₉H₁₂BF₃KN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09993553 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used as a reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its boron-containing structure makes it suitable for palladium-catalyzed coupling with aryl halides, facilitating the preparation of substituted aromatic compounds. Commonly applied in pharmaceutical and agrochemical research for building complex molecules with nitrogen-containing functional groups. The dimethylaminomethyl group enhances solubility and can act as a directing or activating group in multi-step syntheses. Stable under standard conditions and compatible with a variety of reaction conditions, making it a practical choice for late-stage functionalization.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,060.00 |
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| 1.000 | 10-20 days | ฿13,970.00 |
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Potassium (4-((dimethylamino)methyl)phenyl)trifluoroborate
Used as a reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its boron-containing structure makes it suitable for palladium-catalyzed coupling with aryl halides, facilitating the preparation of substituted aromatic compounds. Commonly applied in pharmaceutical and agrochemical research for building complex molecules with nitrogen-containing functional groups. The dimethylaminomethyl group enhances solubility and can act as a directing or activating group in multi-step syntheses. Stable under standard conditions and compatible with a variety of reaction conditions, making it a practical choice for late-stage functionalization.
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