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| | 1,3-Dinitro-2-chloro-5-trifluoromethylbenzene Basic information |
| Product Name: | 1,3-Dinitro-2-chloro-5-trifluoromethylbenzene | | Synonyms: | Benzene, 1-chloro-2,6-dinitro-4-trifluoromethyl;Benzene, 2-chloro-5-(trifluoromethyl)-1,3-dinitro-;Benzotrifluoride, 4-chloro-3,5-dinitro-;Toluene, 4-chloro-3,5-dinitro-alpha,alpha,alpha-trifluoro-;Toluene, 4-chloro-alpha,alpha,alpha-trifluoro-3,5-dinitro-;Trifluoromethyl-3,5-dinitro-4-chlorobenzene;DNT-CL;2-CHLORO-1,3-5-(TRIFLUOROMETHYL)BENZENE | | CAS: | 393-75-9 | | MF: | C7H2ClF3N2O4 | | MW: | 270.55 | | EINECS: | 206-889-3 | | Product Categories: | Intermediate in synthesis of herbicide trifluralin | | Mol File: | 393-75-9.mol |  |
| | 1,3-Dinitro-2-chloro-5-trifluoromethylbenzene Chemical Properties |
| | 1,3-Dinitro-2-chloro-5-trifluoromethylbenzene Usage And Synthesis |
| Chemical Properties | yellow crystalline powder | | Uses | 4-Chloro-3,5-dinitrobenzotrifluoride is used as an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuffs. | | General Description | Yellow crystals. | | Reactivity Profile | A halogenated aromatic nitro compound. Aromatic nitro compounds range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. The aromatic nitro compounds may explode in the presence of a base such as sodium hydroxide or potassium hydroxide even in the presence of water or organic solvents. The explosive tendencies of aromatic nitro compounds are increased by the presence of multiple nitro groups. | | Health Hazard | ACUTE/CHRONIC HAZARDS: Very toxic. Flammable. Irritant. Very hazardous decomposition. |
| | 1,3-Dinitro-2-chloro-5-trifluoromethylbenzene Preparation Products And Raw materials |
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