4-Bromo-2,6-difluorophenol (CAS 104197-13-9)
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4-Bromo-2,6-difluorophenol is a versatile organic compound widely utilized in diverse scientific applications. It is a colorless, crystalline solid that falls into the category of halogenated phenols—a class of organic compounds featuring a hydroxyl group attached to an aromatic ring. In the realm of scientific research, 4-Bromo-2,6-difluorophenol serves as a valuable reagent in organic synthesis and catalyst in the production of organic compounds. Beyond that, this compound finds utility in the analysis of biological samples, including proteins and DNA, and plays a role in polymer and material synthesis. While the full scope of the mechanism of action for 4-Bromo-2,6-difluorophenol is not yet fully understood, researchers have uncovered some significant insights. It is believed to function as an enzyme inhibitor.
4-Bromo-2,6-difluorophenol (CAS 104197-13-9) References
- Small-molecular, non-peptide, non-ATP-competitive polo-like kinase 1 (Plk1) inhibitors with a terphenyl skeleton. | Mita, Y., et al. 2013. Bioorg Med Chem. 21: 608-17. PMID: 23276450
- Structure Property Relationships of Carboxylic Acid Isosteres. | Lassalas, P., et al. 2016. J Med Chem. 59: 3183-203. PMID: 26967507
- Synthesis of Transition-State Inhibitors of Chorismate Utilizing Enzymes from Bromobenzene cis-1,2-Dihydrodiol. | Zhang, XK., et al. 2017. J Org Chem. 82: 3432-3440. PMID: 28282140
- Defining Structure-Functional Selectivity Relationships (SFSR) for a Class of Non-Catechol Dopamine D1 Receptor Agonists. | Martini, ML., et al. 2019. J Med Chem. 62: 3753-3772. PMID: 30875219
- Design, synthesis, and biological evaluation of a new class of histone acetyltransferase p300 inhibitors. | Liu, R., et al. 2019. Eur J Med Chem. 180: 171-190. PMID: 31306905
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
4-Bromo-2,6-difluorophenol, 5 g | sc-261780 | 5 g | $52.00 | |||
4-Bromo-2,6-difluorophenol, 25 g | sc-261780A | 25 g | $321.00 |