Potassium (4-tert-Butoxy carbonylpiperazin-1yl) methyltrifluoroborate
95%
- Product Code: 89285
CAS:
936329-97-4
| Molecular Weight: | 306.17500 g./mol | Molecular Formula: | C₁₀H₁₉BF₃KN₂O₂ |
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| EC Number: | MDL Number: | MFCD10566514 | |
| Melting Point: | 200 °C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a stable and efficient boron reagent, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Its application is significant in pharmaceutical research, where it aids in the development of complex molecules and drug candidates. The compound’s stability and reactivity make it a valuable tool in Suzuki-Miyaura coupling reactions, which are widely used to construct biaryl compounds. Additionally, it is employed in the synthesis of piperazine derivatives, which are key structural motifs in many biologically active compounds. Its trifluoroborate group enhances its compatibility with various reaction conditions, making it a versatile reagent in medicinal chemistry and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $111.14 |
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| 5.000 | 10-20 days | $463.65 |
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Potassium (4-tert-Butoxy carbonylpiperazin-1yl) methyltrifluoroborate
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a stable and efficient boron reagent, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Its application is significant in pharmaceutical research, where it aids in the development of complex molecules and drug candidates. The compound’s stability and reactivity make it a valuable tool in Suzuki-Miyaura coupling reactions, which are widely used to construct biaryl compounds. Additionally, it is employed in the synthesis of piperazine derivatives, which are key structural motifs in many biologically active compounds. Its trifluoroborate group enhances its compatibility with various reaction conditions, making it a versatile reagent in medicinal chemistry and material science.
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