
CAS 35302-70-6: Pinosylvin monomethyl ether
Formula:C15H14O2
InChI:InChI=1S/C15H14O2/c1-17-15-10-13(9-14(16)11-15)8-7-12-5-3-2-4-6-12/h2-11,16H,1H3/b8-7+
InChI key:InChIKey=JVIXPWIEOVZVJC-BQYQJAHWSA-N
SMILES:C(=C/C1=CC=CC=C1)\C2=CC(OC)=CC(O)=C2
Synonyms:- (E)-3-Hydroxy-5-methoxystilbene
- 3-Methoxy-5-[(1E)-2-phenylethenyl]phenol
- 3-Stilbenol, 5-methoxy-
- 5-Methoxy-3-stilbenol
- Phenol, 3-methoxy-5- (2-phenylethenyl)-
- Phenol, 3-methoxy-5-(2-phenylethenyl)-, (E)-
- Phenol, 3-methoxy-5-[(1E)-2-phenylethenyl]-
- Pinosylvin 3-(methyl ether)
- Pinosylvin monomethyl ether
- Pinosylvin, methyl ether
- phenol, 3-methoxy-5-[(E)-2-phenylethenyl]-
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Found 6 products.
Pinosylvin monomethyl ether
CAS:(E)-3-Hydroxy-5-methoxystilbene possesses inhibitory activity against several Gram-positive bacteria, including isolates of methicillin-resistant Staphylococcus aureus (MRSA), Mycobacterium bovis BCG, and avirulent Bacillusanthracis (Sterne strain), amongFormula:C15H14O2Purity:98.00%Color and Shape:SolidMolecular weight:226.2705Pinosylvin monomethyl ether
CAS:Ether phenolFormula:C15H14O2Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:226.28Pinosylvin mono methyl ether
CAS:Pinosylvin mono methyl ether is a phenolic compound, which is a naturally occurring stilbenoid. It is primarily sourced from certain plant species, such as the heartwood of trees in the Pinaceae family. This compound plays a significant role in plant defense, produced by plants as a phytoalexin in response to environmental stressors like pathogens and UV radiation. The mode of action of pinosylvin mono methyl ether involves its ability to interfere with microbial growth due to its antioxidant and antimicrobial properties. It exerts its effects by disrupting cellular processes in microorganisms, including the inhibition of cell membrane function and the impairment of crucial enzymatic activities. In terms of uses and applications, pinosylvin mono methyl ether is utilized in biotechnology and pharmacology for its potential health benefits. It is studied for its antioxidant properties, contributing to the development of treatments targeting oxidative stress-related conditions. Additionally, its antimicrobial characteristics make it a compound of interest for developing preservatives and protective agents in industrial and agricultural settings. Research continues to explore its potential therapeutic applications, including anticancer and anti-inflammatory activities.Formula:C15H14O2Purity:Min. 95%Color and Shape:PowderMolecular weight:226.27 g/mol(E)-3-Methoxy-5-styrylphenol
CAS:Controlled ProductApplications (E)-3-Methoxy-5-styrylphenol (cas# 35302-70-6) is a useful research chemical.Formula:C15H14O2Color and Shape:NeatMolecular weight:226.27Phenol, 3-methoxy-5-[(1E)-2-phenylethenyl]-
CAS:Formula:C15H14O2Purity:97%Color and Shape:SolidMolecular weight:226.2705