Atomfair Acetamide, N-(3-(diethylamino)-4-methoxyphenyl)- C13H20N2O2 CAS 19433-93-3

Description

N-[3-(Diethylamino)-4-methoxyphenyl]acetamide (CAS No. 19433-93-3) is a high-purity organic compound with the molecular formula C₁₃H₂₀N₂O₂. This acetamide derivative features a diethylamino and methoxy substitution on the phenyl ring, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. The compound is supplied as a fine powder or crystalline solid with a purity of ≥98% (HPLC), ensuring consistent performance in laboratory applications. Its well-defined structure and reactivity make it suitable for use in the development of dyes, pigments, and bioactive molecules. Proper storage conditions (room temperature, dry environment) are recommended to maintain stability.

Properties

• CAS Number: 19433-93-3
• Complexity: 242
• IUPAC Name: N-[3-(diethylamino)-4-methoxy-phenyl]acetamide
• InChI: InChI=1S/C13H20N2O2/c1-5-15(6-2)12-9-11(14-10(3)16)7-8-13(12)17-4/h7-9H,5-6H2,1-4H3,(H,14,16)
• InChI Key: BTJCIVXKBILNPY-UHFFFAOYSA-N
• Exact Mass: 236.152477885
• Molecular Formula: C13H20N2O2
• Molecular Weight: 236.31
• SMILES: CCN(CC)C1=C(C=CC(=C1)NC(=O)C)OC
• Topological: 41.6
• Monoisotopic Mass: 236.152477885
• Synonyms: N-[3-(Diethylamino)-4-methoxyphenyl]acetamide, N-(3-(Diethylamino)-4-methoxyphenyl)acetamide, Acetamide, N-[3-(diethylamino)-4-methoxyphenyl]-, EINECS 243-058-4, p-Acetanisidide, 3′-(diethylamino)-, DTXSID1066491, Acetamide, N-(3-(diethylamino)-4-methoxyphenyl)-, DTXCID1036092, 243-058-4, 19433-93-3, 4-Acetylamino-2-(diethylamino)anisole, 3-N,N-Diethylamino-4-methoxyacetanilide, 3′-(Diethylamino)-4′-methoxyacetanilide, SCHEMBL1413103, SCHEMBL11580660, 3-diethylamino-4-methoxy-acetanilide, MFCD01075759, AKOS015890243, AC-11798, 4-Acetylamino-2-(diethylamino)anisole, 97%, NS00026330, G66415, Aetamide, N1-[3-(diethylamino)-4-methoxyphenyl], N-[3-(Diethylamino)-4-methoxyphenyl]acetamide #

Application

N-[3-(Diethylamino)-4-methoxyphenyl]acetamide is primarily used as a key intermediate in the synthesis of dyes and pharmaceutical compounds. Its electron-rich aromatic system makes it suitable for electrophilic substitution reactions, enabling the creation of complex molecular architectures. Researchers also employ this compound in the study of structure-activity relationships (SAR) due to its modifiable functional groups. Additionally, it serves as a precursor in the development of specialty chemicals for analytical and industrial applications.

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