2,2,3,3-Tetrafluoro-1,4-butanediol (CAS 425-61-6)
QUICK LINKS
2,2,3,3-Tetrafluoro-1,4-butanediol is a fluorinated building block in chemical synthesis. It is a precursor for the preparation of various fluorinated compounds. This compound can undergo further chemical reactions to introduce fluorine atoms into organic molecules, leading to the modification of their physicochemical properties. Its mode of action involves participating in nucleophilic substitution reactions, where the hydroxyl groups and fluorine atoms can be selectively replaced with other functional groups. This allows for the creation of new compounds with tailored properties, such as increased lipophilicity or altered reactivity. In the context of research and development, 2,2,3,3-Tetrafluoro-1,4-butanediol plays a role in the design and synthesis of fluorinated molecules for various applications.
2,2,3,3-Tetrafluoro-1,4-butanediol (CAS 425-61-6) References
- Impact of ionic liquid physical properties on lipase activity and stability. | Kaar, JL., et al. 2003. J Am Chem Soc. 125: 4125-31. PMID: 12670234
- Retention of configuration in the nucleophilic substitution reactions of some nine-membered ansa derivatives of cyclotriphosphazatriene. | Beşli, S., et al. 2004. Chemistry. 10: 4915-20. PMID: 15372649
- Properties of phospholipid monolayer deposited on a fluorinated polyurethane. | Wang, LF., et al. 2004. J Biomater Sci Polym Ed. 15: 957-69. PMID: 15461183
- Effect of soft segment length on properties of fluorinated polyurethanes. | Wang, LF. and Wei, YH. 2005. Colloids Surf B Biointerfaces. 41: 249-55. PMID: 15748820
- Alpha-helix formation in melittin and beta-lactoglobulin A induced by fluorinated dialcohols. | Schuh, MD. and Baldwin, MC. 2006. J Phys Chem B. 110: 10903-9. PMID: 16771343
- Comparison of phase structures and surface free energy values for the coatings synthesised from linear polyurethanes and from waterborne polyurethane cationomers. | Król, P., et al. 2011. Colloid Polym Sci. 289: 1757-1767. PMID: 22131639
- Synthesis, cytotoxicity and apoptosis of cyclotriphosphazene compounds as anti-cancer agents. | Yıldırım, T., et al. 2012. Eur J Med Chem. 52: 213-20. PMID: 22483088
- Surface free energy of polyurethane coatings with improved hydrophobicity. | Król, P. and Król, B. 2012. Colloid Polym Sci. 290: 879-893. PMID: 22707844
- Modelling the surface free energy parameters of polyurethane coats-part 1. Solvent-based coats obtained from linear polyurethane elastomers. | Król, P., et al. 2013. Colloid Polym Sci. 291: 1031-1047. PMID: 23525512
- Modelling the surface free energy parameters of polyurethane coats-part 2. Waterborne coats obtained from cationomer polyurethanes. | Król, P., et al. 2014. Colloid Polym Sci. 292: 1051-1059. PMID: 24817782
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2,2,3,3-Tetrafluoro-1,4-butanediol, 5 g | sc-230733 | 5 g | $93.00 |