CAS 16715-79-0
:N-(2,4-Dimethoxyphenyl)-3-oxobutanamide
Description:
N-(2,4-Dimethoxyphenyl)-3-oxobutanamide, with the CAS number 16715-79-0, is an organic compound characterized by its amide functional group and a ketone moiety. This compound features a 2,4-dimethoxyphenyl group, which contributes to its aromatic properties and may influence its reactivity and solubility. The presence of the oxobutanamide structure indicates that it has both carbonyl and amine functionalities, which can participate in various chemical reactions, including nucleophilic additions and condensation reactions. The dimethoxy substituents on the phenyl ring can enhance the compound's lipophilicity and potentially affect its biological activity. Typically, compounds of this nature may exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. Additionally, the molecular structure suggests potential for hydrogen bonding due to the amide group, which can influence its physical properties such as melting point and solubility in different solvents. Overall, N-(2,4-Dimethoxyphenyl)-3-oxobutanamide is a compound with diverse chemical characteristics that may be explored for various applications in research and industry.
Formula:C12H15NO4
InChI:InChI=1S/C12H15NO4/c1-8(14)6-12(15)13-10-5-4-9(16-2)7-11(10)17-3/h4-5,7H,6H2,1-3H3,(H,13,15)
InChI key:InChIKey=IQWUCASGTZCNKK-UHFFFAOYSA-N
SMILES:N(C(CC(C)=O)=O)C1=C(OC)C=C(OC)C=C1
Synonyms:- 2,4-Dimethoxyacetoacetanilide
- Acetoacetanilide, 2′,4′-dimethoxy-
- Butanamide, N-(2,4-dimethoxyphenyl)-3-oxo-
- N-(2,4-dimethoxyphenyl)-3-oxobutanamide
- NSC 50633
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Found 5 products.
2',4'-Dimethoxyacetoacetanilide
CAS:Formula:C12H15NO4Purity:>95.0%(N)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:237.26Butanamide, N-(2,4-dimethoxyphenyl)-3-oxo-
CAS:Formula:C12H15NO4Purity:95%Color and Shape:SolidMolecular weight:237.25182',4'-Dimethoxyacetoacetanilide
CAS:<p>2',4'-Dimethoxyacetoacetanilide is a disubstituted dicarbonyl compound that is synthesized by acetoxylation of 2,4-dimethoxybenzaldehyde. The equilibrium between the two forms can be shifted to favor one form through the addition of reagents, such as dimethylformamide or dicarbonyl compounds. The oxidation of 2',4'-dimethoxyacetoacetanilide with hydrogen peroxide yields 2,4-dihydroxydiphenylmethane, which can undergo hydrolysis with hydrochloric acid to yield phenol.</p>Formula:C12H15NO4Purity:Min. 95%Molecular weight:237.26 g/mol




