CAS 7465-88-5
:4-methoxy-N-phenylbenzamide
Description:
4-Methoxy-N-phenylbenzamide, with the CAS number 7465-88-5, is an organic compound characterized by its amide functional group, which is derived from benzoic acid and an aniline derivative. This compound features a methoxy group (-OCH3) attached to the para position of the benzamide structure, contributing to its chemical properties and reactivity. It typically appears as a solid at room temperature and is soluble in organic solvents such as ethanol and dichloromethane, but may have limited solubility in water due to its hydrophobic aromatic rings. The presence of the methoxy group can influence its electronic properties, potentially enhancing its reactivity in electrophilic aromatic substitution reactions. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Its synthesis generally involves the reaction of an appropriate aniline with a substituted benzoic acid derivative, followed by standard amide formation techniques. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if ingested or inhaled.
Formula:C14H13NO2
InChI:InChI=1/C14H13NO2/c1-17-13-9-7-11(8-10-13)14(16)15-12-5-3-2-4-6-12/h2-10H,1H3,(H,15,16)
SMILES:COc1ccc(cc1)C(=O)Nc1ccccc1
Synonyms:- benzamide, 4-methoxy-N-phenyl-
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Found 5 products.
4-Methoxy-N-phenylbenzamide, 97%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C14H13NO2Purity:97%Molecular weight:227.26N-Phenyl-4-methoxybenzamide
CAS:Formula:C14H13NO2Purity:98%Color and Shape:SolidMolecular weight:227.25854-Methoxy-N-phenyl-benzamide
CAS:<p>4-Methoxy-N-phenyl-benzamide is a biomolecule that belongs to the class of amides. It is synthesized from anilines and amines by coupling with diazo compounds. The reaction mechanism involves the formation of a carbon-nitrogen bond in an electrophilic aromatic substitution reaction. The Langmuir adsorption isotherm technique was used to study the adsorption of 4-methoxybenzamide on copper salt, which has been shown to have high adsorption capacity. This compound also has acidic properties, as it reacts with nitric acid to form a nitro group.</p>Formula:C14H13NO2Purity:Min. 95%Molecular weight:227.26 g/mol




