
CAS 138113-07-2: 2-(7-Methoxy-1-naphthyl)acetamide
Formula:C13H13NO2
InChI:InChI=1S/C13H13NO2/c1-16-11-6-5-9-3-2-4-10(7-13(14)15)12(9)8-11/h2-6,8H,7H2,1H3,(H2,14,15)
SMILES:COc1ccc2cccc(CC(=N)O)c2c1
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Found 7 products.
2-(7-Methoxynaphthalen-1-yl)acetamide
CAS:Formula:C13H13NO2Purity:95%Color and Shape:SolidMolecular weight:215.24787-Methoxy-1-naphthaleneacetamide
CAS:Controlled ProductApplications 7-Methoxy-1-naphthaleneacetamide, can be used for the synthesis of the analogs of Melatonin (M215000), containing naphthalene moiety instead of indole nucleus, having high affinity for the melatonin receptor. Agomelatine Impurity 6 References Tang, J. D., et al.: Org. Prep. Proc. Int., 41, 164 (2009); Sndrieux Y. J., et al.: J. Med. Chem., 35, 1484 (1992);Formula:C13H13NO2Color and Shape:NeatMolecular weight:215.257-Methoxy-1-naphthaleneacetamide
CAS:7-Methoxy-1-naphthaleneacetamide is a chemical compound with the molecular formula CHNO. It is an inhibitor of the enzyme nitroreductase, which is involved in the synthesis of a number of biologically important compounds, including nitric oxide. 7-Methoxy-1-naphthaleneacetamide inhibits nitroaldol and formylation reactions by binding to the active site of the enzyme. This inhibition may be due to steric hindrance or disruption of hydrogen bonds between key amino acid residues in the active site. The pharmacological activity of 7-methoxy-1-naphthaleneacetamide has been studied using 2,2′-(Nitrobenzene)bis(diethylamine), which is used as a substrate for nitroreductase. 7-Methoxy-1-naphthaleneacetamide was found to be an effective inhibitor, with IC50 values ranging from 0.5Formula:C13H13NO2Purity:Min. 95%Molecular weight:215.25 g/mol2-(7-Methoxy-naphthalen-1-yl)acetamide
CAS:2-(7-Methoxy-naphthalen-1-yl)acetamidePurity:95+%Molecular weight:215.25g/mol