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| 2,6-Dichlorobenzal chloride Basic information |
Product Name: | 2,6-Dichlorobenzal chloride | Synonyms: | Benzene, 2,6-dichloro-1-(dichloromethyl);Toluene, alpha,alpha2,6-tetrachloro-;Benzene, 1,3-dichloro-2-(dichloromethyl)-;2,6-Dichlorobenzal chloride,98%;1,3-Dichloro-2-dichloromethylbenzene, 2,6-Dichlorobenzal chloride;2,6,a,a-Tetrachlorotoluene.;A,A,2,6-TETRACHLOROTOLUENE;ALPHA,ALPHA,2,6-TETRACHLOROTOLUENE | CAS: | 81-19-6 | MF: | C7H4Cl4 | MW: | 229.92 | EINECS: | 201-332-0 | Product Categories: | Aryl;Building Blocks;C7;Chemical Synthesis;Halogenated Hydrocarbons;Organic Building Blocks | Mol File: | 81-19-6.mol | |
| 2,6-Dichlorobenzal chloride Chemical Properties |
| 2,6-Dichlorobenzal chloride Usage And Synthesis |
Chemical Properties | clear yellow liquid | Uses | a,a,2,6-Tetrachloro-toluene (Isoconazole Impurity 9) is an impurity of Isoconazole (I798250), an antibacterial and antifungal agent used to treat vaginitis. | General Description | Colorless liquid. | Air & Water Reactions | Insoluble in water. | Reactivity Profile | Simple aromatic halogenated organic compounds, such as 2,6-Dichlorobenzal chloride, are very unreactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Materials in this group may be incompatible with strong oxidizing and reducing agents. Also, they may be incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides. |
| 2,6-Dichlorobenzal chloride Preparation Products And Raw materials |
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