CAS 831-82-3
:4-Fenossiphenolo
- 4-Hydroxydiphenyl ether
- Hydroquinone monophenyl ether
- NSC 25027
- Phenol, 4-Phenoxy-
- Phenol, p-phenoxy-
- o-Phenylhydroquinone
- p-Hydroxydiphenyl ether
- p-Phenoxyphenol
- 4-Phenoxyphenol
4-Phenoxyphenol
CAS:Formula:C12H10O2Purezza:>99.0%(GC)Colore e forma:White to Light yellow to Light orange powder to crystalPeso molecolare:186.214-Phenoxyphenol
CAS:4-PhenoxyphenolFormula:C12H10O2Purezza:97%Colore e forma: white crystalline solidPeso molecolare:186.21g/mol4-Phenoxyphenol
CAS:4-Phenoxyphenol is a phenoxy compound that inhibits bacterial growth by binding to DNA-dependent RNA polymerase, thereby preventing transcription and replication. 4-Phenoxyphenol is synthesized by the reaction of anhydrous sodium with 4-phenoxyphenol in the presence of copper chloride and hydroxyl group. The resulting product has a hydroxyl group attached to the aromatic ring of the phenoxy group. This molecule is then inserted into an expression plasmid with a promoter sequence, which directs it to be expressed in liver cells. The final product can be used as an antibacterial agent against bacteria that are resistant to penicillin, ampicillin, and erythromycin.
Formula:C12H10O2Purezza:Min. 95%Colore e forma:PowderPeso molecolare:186.21 g/mol4-Phenoxyphenol
CAS:Formula:C12H10O2Purezza:97%Colore e forma:Solid, CrystallinePeso molecolare:186.214-Phenoxyphenol
CAS:Prodotto controllatoApplications 4-Phenoxyphenol is a porous organic material with dumbbell channels that appear throughout its structure. These channels can also host solvent molecules during crystal growth. 4-Phenoxyphenol is also part of a group of phenolic compounds that have potential apoptotic activity, which can be used in the development of new treatments for cancer therapy.
References Hansch, C., et al.: Bioorg. Med. Chem., 11, 617 (2003); Thomas, L., et al.: Cryst. Growth. Des., 12, 1746 (2012)Formula:C12H10O2Colore e forma:WhitePeso molecolare:186.21








