Description

Methyl 3-amino-5-methoxybenzoate (CAS No. 217314-47-1) is a high-purity organic compound with the molecular formula C₉H₁₁NO₃. This fine chemical is widely utilized in pharmaceutical and agrochemical research as a key intermediate for the synthesis of complex molecules. The compound features both an amino (-NH₂) and methoxy (-OCH₃) functional group on a benzoate ester scaffold, making it a versatile building block for heterocyclic chemistry and medicinal chemistry applications. Our product is rigorously tested to ensure ≥98% purity by HPLC, with detailed analytical data (NMR, MS) available upon request. Supplied in amber glass vials under inert atmosphere to ensure stability, this compound is ideal for researchers requiring reliable and consistent quality for their synthetic workflows.

Properties

• CAS Number: 217314-47-1
• Complexity: 184
• IUPAC Name: methyl 3-amino-5-methoxy-benzoate
• InChI: InChI=1S/C9H11NO3/c1-12-8-4-6(9(11)13-2)3-7(10)5-8/h3-5H,10H2,1-2H3
• InChI Key: OWMZQNZFHGAVCN-UHFFFAOYSA-N
• Exact Mass: 181.07389321
• Molecular Formula: C9H11NO3
• Molecular Weight: 181.19
• SMILES: COC1=CC(=CC(=C1)N)C(=O)OC
• Topological: 61.6
• Monoisotopic Mass: 181.07389321
• Synonyms: Methyl 3-amino-5-methoxybenzoate, 217314-47-1, MFCD09263221, SCHEMBL414382, DTXSID60474041, Methyl 3-methoxy-5-aminobenzoate, OWMZQNZFHGAVCN-UHFFFAOYSA-N, AKOS006330497, CS-W005930, GS-6513, SY037925, 3-amino-5-methoxy-benzoic acid methyl ester, W16684, EN300-2929147

Application

Methyl 3-amino-5-methoxybenzoate serves as a critical precursor in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and antimicrobial compounds. Its reactive amino group enables facile derivatization for structure-activity relationship (SAR) studies in drug discovery programs. The compound’s benzoate core also finds utility in materials science for the preparation of functionalized aromatic polymers. Researchers value this chemical for its balanced solubility in both polar and non-polar solvents, facilitating diverse reaction conditions.

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