CAS 76425-88-2
:3-[(E)-2-phenylethenyl]phenol
Description:
3-[(E)-2-phenylethenyl]phenol, also known as stilbene phenol, is an organic compound characterized by its phenolic structure and an alkenyl substituent. It features a phenol group attached to a styryl moiety, which contributes to its potential applications in various fields, including materials science and organic synthesis. The compound exhibits a conjugated double bond system, which can impart unique optical properties, making it of interest in photochemistry and as a potential fluorescent dye. Its molecular structure allows for hydrogen bonding due to the hydroxyl (-OH) group, influencing its solubility and reactivity. Additionally, the presence of the phenyl groups can enhance its stability and affect its interaction with other chemical species. As with many organic compounds, its physical properties, such as melting point, boiling point, and solubility, can vary based on environmental conditions and purity. Safety data should be consulted for handling and usage, as phenolic compounds can be hazardous. Overall, 3-[(E)-2-phenylethenyl]phenol is a versatile compound with potential applications in various chemical and industrial processes.
Formula:C14H12O
InChI:InChI=1/C14H12O/c15-14-8-4-7-13(11-14)10-9-12-5-2-1-3-6-12/h1-11,15H/b10-9+
Synonyms:- 3-[(E)-2-Phenylvinyl]phenol
- 3-Stilbenol, (E)-
- Phenol, 3-(2-phenylethenyl)-
- Phenol, 3-(2-phenylethenyl)-, (E)-
- phenol, 3-[(E)-2-phenylethenyl]-
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Found 4 products.
3-[(E)-2-Phenylvinyl]phenol
CAS:Formula:C14H12OPurity:95%Color and Shape:SolidMolecular weight:196.2445trans-3-Hydroxystilbene
CAS:<p>Trans-3-Hydroxystilbene (trans-3HSB) is a natural phenolic compound that has been shown to have anti-cancer effects. This compound inhibits the proliferation of cancer cells and induces apoptosis in pancreatic cancer cells by inhibiting casein kinase 2, which regulates protein synthesis and cell cycle progression. Trans-3HSB also inhibits the expression of survivin, a protein that protects cancer cells from apoptosis. It has chemopreventive effects against skin cancer in mice by inducing caspases and glucuronide conjugate formation.</p>Formula:C14H12OPurity:Min. 95%Color and Shape:PowderMolecular weight:196.24 g/moltrans-3-Hydroxystilbene
CAS:Controlled ProductFormula:C14H12OColor and Shape:NeatMolecular weight:196.244




