Potassium N-cyclohexyl-aminomethyltrifluoroborate
95%
- Product Code: 89420
CAS:
888711-52-2
| Molecular Weight: | 219.098 g./mol | Molecular Formula: | C₇H₁₄BF₃NK |
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| EC Number: | MDL Number: | MFCD10566511 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
Primarily utilized in organic synthesis, this compound serves as a stable and efficient reagent for cross-coupling reactions. It is particularly valuable in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. Its stability under various conditions makes it a preferred choice in pharmaceutical and agrochemical research, where precise and reliable reactions are crucial. Additionally, it is employed in the development of advanced materials, such as polymers and liquid crystals, due to its ability to facilitate complex molecular structures. Its trifluoroborate group enhances reactivity and selectivity, making it a versatile tool in modern synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €150.30 |
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| 1.000 | 10-20 days | €439.97 |
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Potassium N-cyclohexyl-aminomethyltrifluoroborate
Primarily utilized in organic synthesis, this compound serves as a stable and efficient reagent for cross-coupling reactions. It is particularly valuable in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. Its stability under various conditions makes it a preferred choice in pharmaceutical and agrochemical research, where precise and reliable reactions are crucial. Additionally, it is employed in the development of advanced materials, such as polymers and liquid crystals, due to its ability to facilitate complex molecular structures. Its trifluoroborate group enhances reactivity and selectivity, making it a versatile tool in modern synthetic chemistry.
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