CAS 78868-03-8
:N-methyl-2-[1-phenyl-1-(pyridin-2-yl)ethoxy]ethanamine
Description:
N-methyl-2-[1-phenyl-1-(pyridin-2-yl)ethoxy]ethanamine, with the CAS number 78868-03-8, is a chemical compound that belongs to the class of amines. It features a complex structure characterized by a phenyl group and a pyridine ring, which contribute to its potential biological activity. The presence of the N-methyl group indicates that it is a tertiary amine, which can influence its solubility and reactivity. This compound may exhibit properties such as being a potential ligand for various receptors due to its structural motifs, making it of interest in medicinal chemistry and pharmacology. Its specific interactions and effects would depend on the context of its use, including concentration and the biological system involved. As with many organic compounds, it is essential to handle it with care, considering safety protocols and potential toxicity. Further studies would be necessary to fully elucidate its characteristics, including its physical properties, reactivity, and potential applications in research or industry.
Formula:C16H20N2O
InChI:InChI=1/C16H20N2O/c1-16(19-13-12-17-2,14-8-4-3-5-9-14)15-10-6-7-11-18-15/h3-11,17H,12-13H2,1-2H3
SMILES:CC(c1ccccc1)(c1ccccn1)OCCNC
Synonyms:- Ethanamine, N-methyl-2-(1-phenyl-1-(2-pyridinyl)ethoxy)-
- N-Methyl-2-(1-phenyl-1-(2-pyridinyl)ethoxy)ethanamine
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Found 4 products.
N-Desmethyldoxylamine
CAS:<p>Applications N-Desmethyldoxylamine is a metabolite of Doxylamine. It is used as an analyte in hair and urine analysis in drug-faciliated crime. It can also be used as an analyte in human blood plasma for intoxication by doxylamine.<br>References Ganes, D., et al.: Xenobiotica, 17, 993 (1987); Kim, J., et al.: Anal. Bioanal. Chem., 408, 251 (2016); Grobosch, T., et al: GIT Labor Fachz., 55, 116 (2011); Remane, D., et al.: Anal. Bioanal. Chem., 406, 4411 (2014)<br></p>Formula:C16H20N2OColor and Shape:NeatMolecular weight:256.34N-Desmethyldoxylamine
CAS:<p>N-Desmethyldoxylamine is a chemical with a molecular weight of 212.3 g/mol and a melting point of 114 °C. It has been shown to inhibit the growth of human cells in culture, as well as mouse liver cells, by inhibiting the formation of new blood vessels or angiogenesis. N-Desmethyldoxylamine is also used for the treatment of cancerous tumours in animals and humans. This drug binds to epidermal growth factor (EGF) receptors on cell surfaces and blocks the binding of EGF, which prevents cellular proliferation. N-Desmethyldoxylamine has been shown to cause side-chain cleavage reactions at the C2 position on the naphthalene ring and at the methyl group of the methoxy substituent on naphthalene. It can also be metabolized into an epoxide that reacts with DNA bases, leading to DNA damage and inhibition of transcriptional activity.</p>Formula:C16H20N2OPurity:Min. 95%Molecular weight:256.34 g/mol



