| Weight | 251.905 g/mol |
|---|---|
| Formula | C6H4Br2O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,5-DIBROMOPHENOL (28165-52-8)
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- Formation of 2'-hydroxy-2,3',4,5'-tetrabromodipheyl ether (2'-HO-BDE68) from 2,4-dibromophenol in aqueous solution under simulated sunlight irradiation. (Chemosphere, 2011)
- The Mechanism of Nitrosodecarboxylation of 3,5-Dibromo-4-hydroxybenzoic Acid and Nitrosodeprotonation of 2,6-Dibromophenol (Journal of the American Chemical Society, 1962)
- Oxidative degradation of 2,6-dibromophenol using anion-exchange resin supported supramolecular catalysts of iron(III)-5,10,15,20-tetrakis (p-hydroxyphenyl)porphyrin bound to humic acid prepared via formaldehyde and urea-formaldehyde polycondensation (Journal of Environmental Science and Health Part A-toxic\/hazardous Substances & Environmental Engineering, 2010)
- Long range 4J- and 6J-interactions in 2,6-dimethyl-3,4-dibromophenol and 3,5-dimethyl-4-hydroxybenzaldehyde (Tetrahedron Letters, 1968)
- Quantum chemical and direct dynamic study on homogeneous gas-phase formation of PBDD/Fs from 2,4,5-tribromophenol and 3,4-dibromophenol. (Chemosphere, 2013)
- Synthesis and Anion Recognition Properties of 2-(2,4-Dibromophenol)-1H-imidazo[4,5-f][1,10] phenanthroline (Chinese Journal of Synthetic Chemistry, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C(C=C1Br)O)Br
-
InChIKeyGUXWVUVLXIJHQF-UHFFFAOYSA-N
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