|
| 2,6-Dibromophenol Basic information |
Product Name: | 2,6-Dibromophenol | Synonyms: | 2,6-DIBROMOPHENOL;2,6-dibromo-pheno;2,6-DIBROMOPHENOL, 1000MG,NEAT;2 6-DIBROMOPHENOL 99% (HPLC);2,6-Dibromophenol98%;2,6-Dibromophenol,99%;Phenol, 2,6-dibromo-;Dibromophenol, 2,6- | CAS: | 608-33-3 | MF: | C6H4Br2O | MW: | 251.9 | EINECS: | 210-161-0 | Product Categories: | Chemical Class;D;Organic Building Blocks;DAlphabetic;DIA - DIC;Halogenated;Aromatic Phenols;Oxygen Compounds;Phenols;Alpha Sort;BromoVolatiles/ Semivolatiles;bc0001 | Mol File: | 608-33-3.mol | |
| 2,6-Dibromophenol Chemical Properties |
Melting point | 53-56 °C (lit.) | Boiling point | 255-256 °C/740 mmHg (lit.) | density | 1.8854 (rough estimate) | refractive index | 1.5380 (estimate) | Fp | 255-256°C | storage temp. | room temp | solubility | Soluble in DMSO | pka | 6.89±0.10(Predicted) | form | Crystals or Needles | color | White | Water Solubility | Soluble in ethanol and ether. Slightly soluble in water. | λmax | 286nm(EtOH)(lit.) | BRN | 2043614 | InChIKey | SSIZLKDLDKIHEV-UHFFFAOYSA-N | CAS DataBase Reference | 608-33-3(CAS DataBase Reference) | NIST Chemistry Reference | Phenol, 2,6-dibromo-(608-33-3) | EPA Substance Registry System | Phenol, 2,6-dibromo- (608-33-3) |
| 2,6-Dibromophenol Usage And Synthesis |
Chemical Properties | White crystals or needles | Uses | 2,6-Dibromophenol is used in the production of 3,4,5-trimethoxybenzaldehyde and 2-(2,6-dibromophenoxy)ethylbromide. | Uses | 2,6-Dibromophenol is an off-flavor compound that is a metabolite of the spoilage bacteria Alicyclobacillus acidoterrestris. 2,6-Dibromophenol is a metabolic inhibitor and an auxin-like molecule. | Definition | ChEBI: 2,6-dibromophenol is a dibromophenol that is phenol in which both of the hydrogens that are ortho to the phenolic hydroxy group have been replaced by bromines. It has a role as a marine metabolite. It is a bromohydrocarbon and a dibromophenol. It is functionally related to a 1,3-dibromobenzene. | General Description | 2,6-Dibromophenol has been isolated from a luminous marine enteropneust, Balanoglossus biminiensis and is responsible for the characteristic ″iodoform-like″ odor of these animals. | Purification Methods | Distil the phenol under vacuum (at 10mm), then crystallise it from cold CHCl3 or from EtOH/water. [Beilstein 6 H 202, 6 I 106, 6 II 188, 6 III 755, 6 IV 1064.] |
| 2,6-Dibromophenol Preparation Products And Raw materials |
|