Potassium trifluoro(thiomorpholinomethyl)borate
95%
- Product Code: 46764
CAS:
1150654-80-0
| Molecular Weight: | 223.11 g./mol | Molecular Formula: | C₅H₁₀BF₃KNS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD10700162 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized as a reagent in organic synthesis, particularly in the formation of carbon-boron bonds. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura couplings, where it acts as a source of the trifluoroborate anion. This anion is stable and easy to handle, making it a valuable tool for constructing complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its thiomorpholine moiety can impart unique reactivity or selectivity in certain transformations, enhancing its utility in targeted synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿6,822.00 |
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| 1.000 | 10-20 days | ฿13,734.00 |
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| 5.000 | 10-20 days | ฿44,622.00 |
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Potassium trifluoro(thiomorpholinomethyl)borate
This chemical is primarily utilized as a reagent in organic synthesis, particularly in the formation of carbon-boron bonds. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura couplings, where it acts as a source of the trifluoroborate anion. This anion is stable and easy to handle, making it a valuable tool for constructing complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its thiomorpholine moiety can impart unique reactivity or selectivity in certain transformations, enhancing its utility in targeted synthetic pathways.
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