(3,4-Dimethoxyphenyl)acetic acid
(3,4-Dimethoxyphenyl)acetic acid (CAS No.: 93-40-3) is an aromatic phenylacetic acid derivative widely utilized as a versatile intermediate and building block in chemical biology and medicinal chemistry research. Characterized by methoxy-substituted aromatic functionality, this compound serves as a precursor for the construction of phenethylamine-related scaffolds and other bioactive small molecules, supporting the rational design and synthesis of structurally diverse libraries. It is notably employed as an intermediate in the preparation of papaverine-related compounds, thereby contributing to studies focused on smooth muscle modulation and associated signaling pathways, including cyclic nucleotide-mediated processes. In biochemical and pharmacological investigations, it is often used as a metabolic analog to probe biotransformation pathways, receptor–ligand interactions, and structure–activity relationships of related compounds. Although direct molecular targets are not well-defined, analogs derived from this scaffold have been reported to exhibit activity in enzyme and receptor assays within the nanomolar to micromolar range, depending on structural modifications and assay conditions. In vitro and in vivo experimental applications typically involve its incorporation into synthetic schemes or its evaluation in cell-based assays to explore metabolic stability, pathway engagement, and functional activity, with concentrations or dosing regimens adjusted according to specific experimental objectives.
| Physical Appearance | Solid |
| Storage | -20°C |
| M.Wt | 196.2 |
| Cas No. | 93-40-3 |
| Formula | C10H12O4 |
| Solubility | insoluble in H2O; ≥25 mg/mL in EtOH; ≥55 mg/mL in DMSO |
| Chemical Name | 2-(3,4-dimethoxyphenyl)acetic acid |
| Canonical SMILES | COC(C=C1)=C(OC)C=C1CC(O)=O |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |







