potassium cyclopentyl(trifluoro)borate(1-)
98%
- Product Code: 226110
CAS:
1040745-70-7
| Molecular Weight: | 176.0295 g./mol | Molecular Formula: | C₅H₉BF₃K |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04112712 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20℃, inert gas |
Product Description:
Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a source of the cyclopentyl group. Its trifluoroborate structure provides enhanced stability and solubility compared to boronic acids, making it suitable for reactions under aqueous or mild conditions. It enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical intermediates, especially where steric hindrance or functional group tolerance is a concern. The reagent is valued for its ability to introduce cyclopentyl moieties into aromatic or heteroaromatic systems, which are common motifs in bioactive molecules.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 5g | 10-20 days | $63.06 |
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| 10g | 10-20 days | $115.53 |
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| 25g | 10-20 days | $283.52 |
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| 100g | 10-20 days | $1,086.38 |
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potassium cyclopentyl(trifluoro)borate(1-)
Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a source of the cyclopentyl group. Its trifluoroborate structure provides enhanced stability and solubility compared to boronic acids, making it suitable for reactions under aqueous or mild conditions. It enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical intermediates, especially where steric hindrance or functional group tolerance is a concern. The reagent is valued for its ability to introduce cyclopentyl moieties into aromatic or heteroaromatic systems, which are common motifs in bioactive molecules.
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