Chemistry:Tetrachlorocatechol
From HandWiki
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| Names | |
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| Other names
3,4,5,6-Tetrachloro-1,2-benzenediol, Tetrachloropyrocatechol
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| Identifiers | |
3D model (JSmol)
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| 1876366 | |
| ChEBI | |
| ChemSpider | |
| EC Number |
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| 3937 | |
| KEGG | |
PubChem CID
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| UNII | |
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| Properties | |
| C6H2Cl4O2 | |
| Molar mass | 247.88 g·mol−1 |
| Appearance | white solid |
| Density | 1.848 g/cm3 (20 °C) |
| Melting point | 194 °C (381 °F; 467 K) |
| Hazards | |
| GHS pictograms |   
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| GHS Signal word | Danger |
| H302, H318, H400 | |
| P264, P264+265Script error: No such module "Preview warning".Category:GHS errors, P270, P273, P280, P301+317Script error: No such module "Preview warning".Category:GHS errors, P305+354+338Script error: No such module "Preview warning".Category:GHS errors, P317Script error: No such module "Preview warning".Category:GHS errors, P330, P391, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Tracking categories (test):
Tetrachlorocatechol is an organochlorine compound with the formula C
6Cl
4(OH)
2. It is a white solid. It results from the degradation of the controversial pesticide pentachlorophenol.[2] It is a precursor to the reagent TRISPHAT. Its conjugate base also functions as a ligand for transition metals.[3]
References
- ↑ "Tetrachlorocatechol" (in en). https://pubchem.ncbi.nlm.nih.gov/compound/14537#section=Safety-and-Hazards.
- ↑ Oturan, Mehmet A.; Oturan, Nihal; Lahitte, Claude; Trevin, Stéphane (2001). "Production of hydroxyl radicals by electrochemically assisted Fenton's reagent". Journal of Electroanalytical Chemistry 507 (1–2): 96–102. doi:10.1016/S0022-0728(01)00369-2.
- ↑ Ackermann, Jens; Meyer, Franc; Kaifer, Elisabeth; Pritzkow, Hans (2002). "Tuning the Activity of Catechol Oxidase Model Complexes by Geometric Changes of the Dicopper Core". Chemistry - A European Journal 8 (1): 247–258. doi:10.1002/1521-3765(20020104)8:1<247::AID-CHEM247>3.0.CO;2-P. PMID 11822456.
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