Description

Methyl 2-(4-hydroxy-3-nitrophenyl)acetate (CAS No. 61873-93-6) is a high-purity organic compound with the molecular formula C₉H₉NO₅. This nitrophenyl derivative is widely utilized in pharmaceutical and chemical research due to its reactive phenolic and ester functional groups. The compound is characterized by its crystalline solid form and is soluble in common organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO). With an IUPAC name of methyl 2-(4-hydroxy-3-nitrophenyl)acetate, it serves as a key intermediate in the synthesis of fine chemicals, dyes, and active pharmaceutical ingredients (APIs). Our product is rigorously tested for purity (typically ≥95% by HPLC) and is supplied with comprehensive analytical data, including ¹H NMR and MS spectra, ensuring reliability for your research needs.

Properties

• CAS Number: 61873-93-6
• Complexity: 249
• IUPAC Name: methyl 2-(4-hydroxy-3-nitro-phenyl)acetate
• InChI: InChI=1S/C9H9NO5/c1-15-9(12)5-6-2-3-8(11)7(4-6)10(13)14/h2-4,11H,5H2,1H3
• InChI Key: SPCRIUSIYZYZKN-UHFFFAOYSA-N
• Exact Mass: 211.04807239
• Molecular Formula: C9H9NO5
• Molecular Weight: 211.17
• SMILES: COC(=O)CC1=CC(=C(C=C1)O)[N+](=O)[O-]
• Topological: 92.4
• Monoisotopic Mass: 211.04807239
• Synonyms: 61873-93-6, methyl 2-(4-hydroxy-3-nitrophenyl)acetate, DTXSID40363025, DTXCID40314072, Methyl (4-Hydroxy-3-nitrophenyl)acetate, 4-Hydroxy-3-nitro-phenylacetic acid methl ester, Methyl (4-Hydroxy-3-nitrophenyl)acetate, MFCD04125034, methyl 4-hydroxy-3-nitrophenylacetate, 4-(2-Methoxy-2-oxoethyl)-2-nitrophenol, SCHEMBL286994, METHYL (4-HYDROXY-3-NITROPHENYL)ACETATE 95%, SPCRIUSIYZYZKN-UHFFFAOYSA-N, SBB053725, methyl 3-nitro-4-hydroxyphenylacetate, AKOS005070116, CS-W000710, Methyl(4-hydroxy-3-nitrophenyl)acetate, methyl2-(4-hydroxy-3-nitrophenyl)acetate, SY103835, methyl-2-(4-hydroxy-3-nitrophenyl)acetate, ST50949689, 2-Hydroxy-5-(2-methoxy-2-oxoethyl)nitrobenzene, 2X-0875, SR-01000307011, SR-01000307011-1

Application

Methyl 2-(4-hydroxy-3-nitrophenyl)acetate is primarily employed as a versatile building block in organic synthesis, particularly in the development of pharmaceutical intermediates and agrochemicals. Its reactive nitro and hydroxyl groups make it suitable for further functionalization via reduction, alkylation, or coupling reactions. Researchers also utilize this compound in the study of nitroaromatic chemistry and as a precursor for dyes or pigments. Its stability and well-defined structure lend it to applications in material science and analytical method development.

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