
CAS 134029-62-2
:(E)-3,4,5,4′-Tetramethoxystilbene
Description:
(E)-3,4,5,4′-Tetramethoxystilbene is an organic compound characterized by its stilbene backbone, which features a trans configuration (indicated by the (E) designation). This compound contains four methoxy groups (-OCH₃) attached to the aromatic rings, contributing to its unique chemical properties and potential biological activities. The presence of these methoxy substituents enhances its solubility in organic solvents and may influence its reactivity and interaction with biological targets. The compound is of interest in various fields, including medicinal chemistry and materials science, due to its potential antioxidant and anticancer properties. Its structural features suggest that it may exhibit interesting photophysical properties, making it a candidate for applications in organic electronics or as a fluorescent probe. As with many stilbene derivatives, (E)-3,4,5,4′-Tetramethoxystilbene may also undergo isomerization under certain conditions, which can affect its stability and reactivity. Overall, this compound represents a fascinating area of study within organic chemistry and its applications.
Formula:C18H20O4
InChI:InChI=1S/C18H20O4/c1-19-15-9-7-13(8-10-15)5-6-14-11-16(20-2)18(22-4)17(12-14)21-3/h5-12H,1-4H3/b6-5+
InChI key:InChIKey=GGFQQRXTLIJXNY-AATRIKPKSA-N
SMILES:O(C)C1=C(OC)C(OC)=CC(/C=C/C2=CC=C(OC)C=C2)=C1
Synonyms:- DMU 212
- 1,2,3-Trimethoxy-5-[(1E)-2-(4-methoxyphenyl)ethenyl]benzene
- Benzene, 1,2,3-trimethoxy-5-[(1E)-2-(4-methoxyphenyl)ethenyl]-
- (E)-3,4,5,4′-Tetramethoxystilbene
- Benzene, 1,2,3-trimethoxy-5-[2-(4-methoxyphenyl)ethenyl]-, (E)-
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Found 4 products.
DMU-212
CAS:<p>DMU-212, a Resveratrol derivative, has antimitotic, antiproliferative, antioxidant properties; induces apoptosis via ERK1/2.</p>Formula:C18H20O4Purity:99.86%Color and Shape:SolidMolecular weight:300.35trans-3,4,5,4'-Tetramethoxystilbene
CAS:<p>Trans-3,4,5,4'-tetramethoxystilbene is a potential anti-cancer drug that inhibits the growth of prostate cancer cells. It has been shown to inhibit the activity of cytochrome P450 enzymes and induce apoptosis in prostate cancer cells. Trans-3,4,5,4'-tetramethoxystilbene also has an inhibitory effect on angiogenesis and induces apoptosis in breast cancer cells. This compound is not readily absorbed from the gastrointestinal tract and has low bioavailability due to its chemical properties. Trans-3,4,5,4'-tetramethoxystilbene binds to DNA and inhibits transcription by competitive inhibition of RNA polymerase II and III.</p>Formula:C18H20O4Purity:Min. 95%Color and Shape:PowderMolecular weight:300.35 g/moltrans-3,4,5,4'-Tetramethoxystilbene
CAS:Controlled Product<p>Applications trans-3,4,5,4'-Tetramethoxystilbene (cas# 134029-49-5) is a useful research chemical.<br></p>Formula:C18H20O4Color and Shape:White To Off-WhiteMolecular weight:300.349



