(1-(Ethoxycarbonyl)cyclopropyl)triphenylphosphonium tetrafluoroborate
98%
- Product Code: 36128
CAS:
52186-89-7
| Molecular Weight: | 462.23 g./mol | Molecular Formula: | C₂₄H₂₄BF₄O₂P |
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| EC Number: | MDL Number: | MFCD00051879 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This chemical is primarily used in organic synthesis as a reagent for the formation of cyclopropane rings, which are important structural motifs in many pharmaceuticals and agrochemicals. It acts as a precursor in the synthesis of cyclopropane derivatives through reactions like the Corey-Chaykovsky reaction, where it facilitates the transfer of a cyclopropyl group to various electrophiles. The compound is particularly valuable in the development of complex organic molecules, including natural products and bioactive compounds, due to its ability to introduce cyclopropane rings with high selectivity and efficiency. Additionally, its tetrafluoroborate counterion enhances solubility and stability, making it suitable for use in a wide range of reaction conditions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,816.00 |
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| 5.000 | 10-20 days | ฿9,198.00 |
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| 10.000 | 10-20 days | ฿17,091.00 |
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| 25.000 | 10-20 days | ฿38,295.00 |
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(1-(Ethoxycarbonyl)cyclopropyl)triphenylphosphonium tetrafluoroborate
This chemical is primarily used in organic synthesis as a reagent for the formation of cyclopropane rings, which are important structural motifs in many pharmaceuticals and agrochemicals. It acts as a precursor in the synthesis of cyclopropane derivatives through reactions like the Corey-Chaykovsky reaction, where it facilitates the transfer of a cyclopropyl group to various electrophiles. The compound is particularly valuable in the development of complex organic molecules, including natural products and bioactive compounds, due to its ability to introduce cyclopropane rings with high selectivity and efficiency. Additionally, its tetrafluoroborate counterion enhances solubility and stability, making it suitable for use in a wide range of reaction conditions.
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