CAS 5531-98-6
:3,4-Dimethoxy-N,N-dimethyl-1-phenanthreneethanamine
Description:
3,4-Dimethoxy-N,N-dimethyl-1-phenanthreneethanamine, with the CAS number 5531-98-6, is a chemical compound that belongs to the class of phenanthrene derivatives. It features a phenanthrene backbone, which is a polycyclic aromatic hydrocarbon, and is substituted with two methoxy groups and a dimethylamino group. The presence of methoxy groups typically enhances the compound's solubility in organic solvents and can influence its electronic properties, potentially making it useful in various applications, including organic electronics and as a fluorescent probe. The dimethylamino group may impart basicity and can participate in hydrogen bonding, affecting the compound's reactivity and interaction with biological systems. This compound may exhibit interesting photophysical properties due to its aromatic structure, which can be relevant in studies of light absorption and emission. However, detailed information regarding its specific applications, toxicity, and environmental impact would require further investigation and analysis.
Formula:C20H23NO2
InChI:InChI=1S/C20H23NO2/c1-21(2)12-11-15-13-18(22-3)20(23-4)19-16-8-6-5-7-14(16)9-10-17(15)19/h5-10,13H,11-12H2,1-4H3
InChI key:InChIKey=UZZFAUDNCIFFPM-UHFFFAOYSA-N
SMILES:O(C)C=1C=2C(C(CCN(C)C)=CC1OC)=CC=C3C2C=CC=C3
Synonyms:- 1-Phenanthreneethylamine, 3,4-dimethoxy-N,N-dimethyl-
- 1-phenanthreneethanamine, 3,4-dimethoxy-N,N-dimethyl-
- 3,4-Dimethoxy-N,N-dimethyl-1-phenanthreneethanamine
- Atherosperminine
- NSC 93678
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Found 5 products.
Atherosperminine
CAS:<p>Atherosperminine inhibits AChE/BChE and relaxes trachealis via cAMP phosphodiesterase inhibition.</p>Formula:C20H23NO2Purity:99.92%Color and Shape:SolidMolecular weight:309.4Atherosperminine
CAS:Controlled Product<p>Atherosperminine is an alkaloid compound, which is a bioactive chemical derived from plants. Specifically, it is sourced from members of the Lauraceae family, such as Atherosperma moschatum. This compound exhibits a range of pharmacological activities that are of significant interest to researchers. The mode of action of atherosperminine involves interactions with various biological pathways, potentially affecting physiological processes and exhibiting therapeutic effects.</p>Formula:C20H23NO2Purity:Min. 95%Molecular weight:309.4 g/mol




