2,3,4,5,6-Pentafluorobenzoyl chloride
99%
- Product Code: 67738
Alias:
2,3,4,5,6-Pentafluorobenzoyl chloride
Pentafluorobenzoyl chloride
Pentafluorobenzoyl chloride
CAS:
2251-50-5
| Molecular Weight: | 230.52 g./mol | Molecular Formula: | C₆F₅COCl |
|---|---|---|---|
| EC Number: | 218-842-4 | MDL Number: | MFCD00000657 |
| Melting Point: | Boiling Point: | 158-159 °C(lit.) | |
| Density: | 1.601 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C, dry, sealed |
Product Description:
Used primarily as a reagent in organic synthesis, this compound is highly effective for introducing pentafluorobenzoyl groups into various molecules. It is commonly employed in the preparation of derivatives for analytical purposes, particularly in gas chromatography and mass spectrometry, where it enhances the detectability of compounds due to the electron-withdrawing properties of the pentafluorobenzoyl group. Additionally, it finds application in the development of pharmaceuticals and agrochemicals, where it aids in the modification of molecules to improve their stability, reactivity, or bioavailability. Its use in peptide chemistry is also notable, as it helps in the protection of amino groups during synthesis.
Product Specification:
| Test | Specification |
|---|---|
| PurityGC | 98.5 100% |
| REFRACTIVE INDEX N20D | 1.452-1.454 |
| SPECIFIC GRAVITY 2020C | 1.666-1.671 |
| APPEARANCE | Colorless to light yellow liquid |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $16.20 |
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| 5.000 | 10-20 days | $44.85 |
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| 25.000 | 10-20 days | $123.76 |
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| 100.000 | 10-20 days | $406.98 |
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2,3,4,5,6-Pentafluorobenzoyl chloride
Used primarily as a reagent in organic synthesis, this compound is highly effective for introducing pentafluorobenzoyl groups into various molecules. It is commonly employed in the preparation of derivatives for analytical purposes, particularly in gas chromatography and mass spectrometry, where it enhances the detectability of compounds due to the electron-withdrawing properties of the pentafluorobenzoyl group. Additionally, it finds application in the development of pharmaceuticals and agrochemicals, where it aids in the modification of molecules to improve their stability, reactivity, or bioavailability. Its use in peptide chemistry is also notable, as it helps in the protection of amino groups during synthesis.
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