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Atomfair Methyl 2-(4-methoxy-3-nitrophenyl)acetate C10H11NO5 CAS 34837-88-2
Methyl 2-(4-methoxy-3-nitrophenyl)acetate (CAS No. 34837-88-2) is a high-purity organic compound with the molecular formula C10H11NO5. This ester derivative features a methoxy and nitro functional group on the phenyl ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 225.20 g/mol , it is commonly used in the development of fine chemicals, agrochemicals, and active pharmaceutical ingredients (APIs). Our product is rigorously tested for purity and stability, ensuring optimal performance in sensitive applications. Available in various packaging options, it is ideal for researchers requiring precise and reliable reagents.
Description
Methyl 2-(4-methoxy-3-nitrophenyl)acetate (CAS No. 34837-88-2) is a high-purity organic compound with the molecular formula C10H11NO5. This ester derivative features a methoxy and nitro functional group on the phenyl ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 225.20 g/mol, it is commonly used in the development of fine chemicals, agrochemicals, and active pharmaceutical ingredients (APIs). Our product is rigorously tested for purity and stability, ensuring optimal performance in sensitive applications. Available in various packaging options, it is ideal for researchers requiring precise and reliable reagents.
Properties
- CAS Number: 34837-88-2
- Complexity: 262
- IUPAC Name: methyl 2-(4-methoxy-3-nitro-phenyl)acetate
- InChI: InChI=1S/C10H11NO5/c1-15-9-4-3-7(6-10(12)16-2)5-8(9)11(13)14/h3-5H,6H2,1-2H3
- InChI Key: HAFCSCBORMDMFL-UHFFFAOYSA-N
- Exact Mass: 225.06372245
- Molecular Formula: C10H11NO5
- Molecular Weight: 225.20
- SMILES: COC1=C(C=C(C=C1)CC(=O)OC)[N+](=O)[O-]
- Topological: 81.4
- Monoisotopic Mass: 225.06372245
- Synonyms: methyl 2-(4-methoxy-3-nitrophenyl)acetate, 34837-88-2, 4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER, MFCD09754963, CHEMBL453034, SCHEMBL6986744, SCHEMBL14684960, DTXSID70551150, HAFCSCBORMDMFL-UHFFFAOYSA-N, SBB096808, AKOS000296335, AD-0713, Methyl (4-methoxy-3-nitrophenyl)acetate, methyl 2-(3-nitro4-methoxyphenyl)acetate, methyl2-(4-methoxy-3-nitrophenyl)acetate
Application
Methyl 2-(4-methoxy-3-nitrophenyl)acetate serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. It is utilized in the preparation of nitroaromatic compounds, which are precursors to dyes, fragrances, and bioactive agents. Researchers also employ this ester in coupling reactions and as a building block for heterocyclic chemistry. Its stability and reactivity make it suitable for multi-step synthetic pathways.
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