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Trichloroacetyl chloride CAS 76-02-8
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Trichloroacetyl chloride
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C2Cl4O
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200KG/Drum
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Colorless liquid
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76-02-8
| CAS NO. | 76-02-8 |
| Alias | TCC |
| Molecular Formula | C2Cl4O |
| Appearance | colorless liquid |
| ASSAY | ≥98% |
| Package | 200KG/Drum |
| PackingGroup | II |
| UN NO. | 2442 |
| HazardClass | 8 |
| Trichloroacetyl chloride (TCC) is produced by reacting trichloroacetic acid with thionyl chloride. The process yields TCC and releases sulfur dioxide gas as a byproduct. TCC serves as a potent acylating agent in organic synthesis, introducing trichloroacetyl groups into various compounds. It finds applications in pharmaceuticals, pesticides, and other chemical reactions. Due to its reactivity and hazardous nature, TCC is handled with caution in specialized laboratory settings by trained professionals. |
Trichloroacetyl chloride (TCC) is used as a potent acylating agent in various chemical reactions. It finds applications in organic synthesis, particularly in pharmaceuticals and pesticide production. TCC introduces trichloroacetyl groups into compounds, leading to the formation of new derivatives. However, its reactivity and hazardous properties necessitate careful handling in specialized laboratory settings by trained professionals. |
| CAS NO. | 76-02-8 |
| Alias | TCC |
| Molecular Formula | C2Cl4O |
| Appearance | colorless liquid |
| ASSAY | ≥98% |
| Package | 200KG/Drum |
| PackingGroup | II |
| UN NO. | 2442 |
| HazardClass | 8 |
| Trichloroacetyl chloride (TCC) is produced by reacting trichloroacetic acid with thionyl chloride. The process yields TCC and releases sulfur dioxide gas as a byproduct. TCC serves as a potent acylating agent in organic synthesis, introducing trichloroacetyl groups into various compounds. It finds applications in pharmaceuticals, pesticides, and other chemical reactions. Due to its reactivity and hazardous nature, TCC is handled with caution in specialized laboratory settings by trained professionals. |
Trichloroacetyl chloride (TCC) is used as a potent acylating agent in various chemical reactions. It finds applications in organic synthesis, particularly in pharmaceuticals and pesticide production. TCC introduces trichloroacetyl groups into compounds, leading to the formation of new derivatives. However, its reactivity and hazardous properties necessitate careful handling in specialized laboratory settings by trained professionals. |
