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| | Tetrachloro-o-benzoquinone Basic information |
| Product Name: | Tetrachloro-o-benzoquinone | | Synonyms: | 3,4,5,6-Tetrachlorocyclohexa-3,5-diene-1,2-dione;Tetrachloro-3,5-cyclohexadiene-1,2-dione;Tetrachloro-o-benzoquinone,97%;Tetrachloro-o-benzoquinone ,96%;3,4,5,6-Tetrachlorocyclohexa-3,5-diene-1,2-dione, o-Chloranil;Tetrachloro-o-benzoquinone, 97% 25GR;Tetrachloro-o-benzoquinone, 97% 5GR;3,4,5,6-Tetrachloro-1,2-benzoquinone 97% | | CAS: | 2435-53-2 | | MF: | C6Cl4O2 | | MW: | 245.88 | | EINECS: | 219-424-4 | | Product Categories: | Pesticide intermediate;Bi (Bismuth) Compounds;Classes of Metal Compounds;New Oxidation of primary & secondary Alcohols;Synthetic Organic Chemistry;Semimetal Compounds;Carbon Radical Producing Catalysts (Environmentally-friendly Oxidation);Environmentally-friendly Oxidation;Oxidation | | Mol File: | 2435-53-2.mol |  |
| | Tetrachloro-o-benzoquinone Chemical Properties |
| | Tetrachloro-o-benzoquinone Usage And Synthesis |
| Chemical Properties | bordeaux fine crystalline powder | | Uses | o-Chloranil is used as a reagent in the synthesis of fused triazolotriazines and triazolotriazepines which exhibit antibacterial activity. Also used as a reagent in the synthesis of nickel diimine catecholate charge-transfer complexes. | | Synthesis Reference(s) | The Journal of Organic Chemistry, 46, p. 3056, 1981 DOI: 10.1021/jo00328a013 | | Purification Methods | Crystallise o-chloranil from AcOH. Dry it in vacuum desiccator over KOH. [Beilstein 7 IV 2068.] |
| | Tetrachloro-o-benzoquinone Preparation Products And Raw materials |
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