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| Name | 3-FLUOROBENZENESULFONYL CHLORIDE |
| Category | Fine chemicals |
| Basic Information | |
| Synonyms | 3-FLUOROBENZENESULFONYL CHLORIDE; |
| CAS number | 701-27-9 |
| EINECS | 628-370-4 |
| Formula | C6H4ClFO2S |
| Structure |  |
| Molecular Weight | 194.61 |
| Melting Point | 7°C |
| Flashing Point | >230 °F |
| Boiling point | 231-232 °C(lit.) |
| Density | 1.463 g/mL at 25 °C(lit.) |
| COA Information | |
| Apperance | Grey-brown to dark brown Powder |
| Purity | min. 99% |
| Moisture | max. 1.0% |
| Safety Information | |
| Hazard Codes | C,Xi |
| Risk Statements | 34-29-14-36/37/38 |
| HazardClass | 8 |
| Safety Statements | 26-36/37/39-45-8-30-23-27 |
| WGK Germany | 3 |
| RIDADR | UN 3265 8/PG 2 |
| HS Code | 29333990 |
| Description | |
| 2,2,6,6-tetramethyl-4-piperidone is an organic compound with the formula OC(CH2CMe2)2NH (where Me = CH3). It is a colorless or white solid that melts near room temperature. The compound is an intermediate in the preparation of 2,2,6,6-tetramethylpiperidine, a sterically hindered base and precursor to the reagent called TEMPO. Triacetonamine is formed by the poly-aldol condensation of acetone in the presence of ammonia and calcium chloride. | |
| Name | 3-FLUOROBENZENESULFONYL CHLORIDE |
| Category | Fine chemicals |
| Basic Information | |
| Synonyms | 3-FLUOROBENZENESULFONYL CHLORIDE; |
| CAS number | 701-27-9 |
| EINECS | 628-370-4 |
| Formula | C6H4ClFO2S |
| Structure | |
| Molecular Weight | 194.61 |
| Melting Point | 7°C |
| Flashing Point | >230 °F |
| Boiling point | 231-232 °C(lit.) |
| Density | 1.463 g/mL at 25 °C(lit.) |
| COA Information | |
| Apperance | Grey-brown to dark brown Powder |
| Purity | min. 99% |
| Moisture | max. 1.0% |
| Safety Information | |
| Hazard Codes | C,Xi |
| Risk Statements | 34-29-14-36/37/38 |
| HazardClass | 8 |
| Safety Statements | 26-36/37/39-45-8-30-23-27 |
| WGK Germany | 3 |
| RIDADR | UN 3265 8/PG 2 |
| HS Code | 29333990 |
| Description | |
| 2,2,6,6-tetramethyl-4-piperidone is an organic compound with the formula OC(CH2CMe2)2NH (where Me = CH3). It is a colorless or white solid that melts near room temperature. The compound is an intermediate in the preparation of 2,2,6,6-tetramethylpiperidine, a sterically hindered base and precursor to the reagent called TEMPO. Triacetonamine is formed by the poly-aldol condensation of acetone in the presence of ammonia and calcium chloride. | |
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