1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)
95%
- Product Code: 126810
Alias:
Selectfluor® fluoride reagent; selective fluoride reagent, N-fluoro-N'-(chloromethyl)triethylenediamine bis(tetrafluoroborate), 1-chloromethyl-4-fluoro-1,4-di Azabicyclo[2.2.2]octane bis(tetrafluoroborate) salt
CAS:
140681-55-6
| Molecular Weight: | 354.26 g./mol | Molecular Formula: | C₇H₁₄B₂ClF₉N₂ |
|---|---|---|---|
| EC Number: | 414-380-4 | MDL Number: | MFCD00142607 |
| Melting Point: | 260 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This chemical is primarily utilized as a highly effective electrophilic fluorinating agent in organic synthesis. It is particularly valuable for introducing fluorine atoms into various organic compounds, a process that is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its ability to selectively fluorinate complex molecules makes it a preferred choice in the preparation of fluorinated intermediates, which often exhibit enhanced biological activity, stability, and metabolic resistance. Additionally, it is employed in the synthesis of radiolabeled compounds for positron emission tomography (PET) imaging, aiding in medical diagnostics and research. Its robust reactivity and efficiency in fluorination reactions contribute significantly to advancements in medicinal chemistry and material science.
Product Specification:
| Test | Specification |
|---|---|
| Purity (Iodometric Titration) | 94.5-105.5 |
| Melting Point (Degree Celsius) | 258-265 |
| Appearance | White To Light Yellow Powder |
| Infrared Spectrum | Conforms To Structure |
| 1H-NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | Ft3,232.23 |
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| 25.000 | 10-20 days | Ft4,525.13 |
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| 100.000 | 10-20 days | Ft13,252.15 |
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| 500.000 | 10-20 days | Ft56,887.29 |
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1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)
This chemical is primarily utilized as a highly effective electrophilic fluorinating agent in organic synthesis. It is particularly valuable for introducing fluorine atoms into various organic compounds, a process that is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its ability to selectively fluorinate complex molecules makes it a preferred choice in the preparation of fluorinated intermediates, which often exhibit enhanced biological activity, stability, and metabolic resistance. Additionally, it is employed in the synthesis of radiolabeled compounds for positron emission tomography (PET) imaging, aiding in medical diagnostics and research. Its robust reactivity and efficiency in fluorination reactions contribute significantly to advancements in medicinal chemistry and material science.
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