Description

Ethyl 3-(4-methoxyphenyl)propanoate (CAS No. 22767-72-2) is a high-purity ester compound with the molecular formula C₁₂H₁₆O₃. This fine chemical is characterized by its clear to pale-yellow appearance and is widely utilized in organic synthesis and pharmaceutical research. Its IUPAC name, ethyl 3-(4-methoxyphenyl)propanoate, reflects its structural composition featuring a methoxyphenyl group and an ethyl ester moiety. The compound is supplied with detailed analytical certificates (including GC/MS, HPLC, and NMR) to ensure quality and consistency for research applications. Suitable for use as a flavor/fragrance intermediate or as a building block in heterocyclic chemistry, it is stored under inert conditions to maintain stability.

Properties

• CAS Number: 22767-72-2
• Complexity: 183
• IUPAC Name: ethyl 3-(4-methoxyphenyl)propanoate
• InChI: InChI=1S/C12H16O3/c1-3-15-12(13)9-6-10-4-7-11(14-2)8-5-10/h4-5,7-8H,3,6,9H2,1-2H3
• InChI Key: BDSDTKZBFYSNLI-UHFFFAOYSA-N
• Exact Mass: 208.109944368
• Molecular Formula: C12H16O3
• Molecular Weight: 208.25
• SMILES: CCOC(=O)CCC1=CC=C(C=C1)OC
• Topological: 35.5
• Monoisotopic Mass: 208.109944368
• Synonyms: Ethyl 3-(4-methoxyphenyl)propanoate, 22767-72-2, Ethyl-p-methoxyhydrocinnamate, MFCD02258632, Ethyl p-methoxyhydrocinnamate; NSC 408331, ethyl3-(4-methoxyphenyl)propanoate, Hydrocinnamic acid, p-methoxy-, ethyl ester, Ethyl 4-methoxybenzenepropanoate, 3-(4-Methoxyphenyl)propionic acid ethyl ester, Benzenepropanoic acid, 4-methoxy-, ethyl ester, SCHEMBL490909, DTXSID40325042, HY-N3869, ethyl 3-(4-methoxyphenyl)propionate, NSC408331, AKOS008949214, Ethyl 3-(4-methoxyphenyl)propanoate #, NSC-408331, AS-62150, DA-07916, SY279048, CS-0024377, 3-(4-methoxyphenyl)-propionic acid ethyl ester, F52655

Application

Ethyl 3-(4-methoxyphenyl)propanoate serves as a versatile intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty fragrances. Its methoxyphenyl group makes it valuable for constructing bioactive molecules targeting CNS disorders or inflammation. Researchers also employ it in coupling reactions to develop novel ester derivatives for material science applications.

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