N-(2,5-Dimethoxyphenyl)acetamide, with the CAS number 3467-59-2, is an organic compound characterized by its acetamide functional group attached to a 2,5-dimethoxyphenyl moiety. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as ethanol and dimethyl sulfoxide, but may have limited solubility in water. The presence of methoxy groups on the aromatic ring contributes to its electronic properties, potentially influencing its reactivity and interactions in various chemical environments. N-(2,5-Dimethoxyphenyl)acetamide may be of interest in medicinal chemistry and research due to its structural similarity to other biologically active compounds. Its synthesis generally involves acylation reactions, and it may be studied for its potential pharmacological effects or as a precursor in the synthesis of more complex molecules. As with any chemical substance, proper handling and safety precautions should be observed, particularly in laboratory settings.

N-(2,5-Dimethoxyphenyl)acetamide

3467-59-2: 2',5'-Dimethoxyacetanilide, 2,5-Dimethoxyacetanilide, 2-Acetamidohydroquinone dimethyl ether, Acetamide, N-(2,5-dimethoxyphenyl)-, Acetanilide, 2′,5′-dimethoxy-, N-(2,5-dimethoxy phenyl)-acetamide, N-(2,5-dimethoxyphenyl)acetamide, NSC 408044,   

2',5'-Dimethoxyacetanilide is a molecule that belongs to the class of organometallic compounds. It is prepared by demethylation of 2,5-dimethoxybenzaldehyde. The carbolines are synthesized from this compound by reaction with ammonium nitrate in presence of halides and intramolecular hydrogen. This compound has been shown to act as a ligand for dopamine receptors.

CAS 3467-59-2: N-(2,5-Dimethoxyphenyl)acetamide

2',5'-Dimethoxyacetanilide

Ref: 3D-DAA46759

N-(2,5-Dimethoxyphenyl)acetamide

Ref: IN-DA003FYU

2',5'-Dimethoxyacetanilide

Ref: 3B-D1671

N-(2,5-dimethoxyphenyl)acetamide

Ref: 10-F720652

2',5'-Dimethoxyacetanilide

Ref: 54-OR950209