Description
Methyl 2-(4-nitrophenyl)acetate (CAS No. 2945-08-6) is a high-purity organic compound with the molecular formula C9H9NO4. This ester derivative of 4-nitrophenylacetic acid is widely used in chemical synthesis, pharmaceutical research, and material science applications. Its nitrophenyl group enhances reactivity, making it a valuable intermediate for coupling reactions, esterifications, and as a precursor for fine chemicals. Our product is rigorously tested for purity and consistency, ensuring optimal performance in sensitive applications. Supplied in sealed containers to maintain stability, it is ideal for laboratory and industrial use.
Properties
- CAS Number: 2945-08-6
- Complexity: 215
- IUPAC Name: methyl 2-(4-nitrophenyl)acetate
- InChI: InChI=1S/C9H9NO4/c1-14-9(11)6-7-2-4-8(5-3-7)10(12)13/h2-5H,6H2,1H3
- InChI Key: PQRGTRBYCFLHKY-UHFFFAOYSA-N
- Exact Mass: 195.05315777
- Molecular Formula: C9H9NO4
- Molecular Weight: 195.17
- SMILES: COC(=O)CC1=CC=C(C=C1)[N+](=O)[O-]
- Topological: 72.1
- Monoisotopic Mass: 195.05315777
- Synonyms: methyl 2-(4-nitrophenyl)acetate, 2945-08-6, Benzeneacetic acid, 4-nitro-, methyl ester, Methyl p-nitrophenylacetate, Methyl (4-nitrophenyl)acetate, METHYL 4-NITROPHENYLACETATE, MFCD00024802, p-Nitrophenylacetic acid, methyl ester, QMK2BOL4OA, 4-Nitrophenylacetic acid methyl ester, NSC-112387, Methyl 4-nitrobenzeneacetate, 4-Nitrophenylacetic acid methyl ester [MI], Methylp-nitrophenylacetate, UNII-QMK2BOL4OA, SCHEMBL521069, methyl2-(4-nitrophenyl)acetate, DTXSID90296874, AB7569, NSC112387, STL420577, (p-Nitrophenyl)acetic acid methylester, AKOS000796551, AS-44854, SY024164, (4-nitro-phenyl)-acetic acid methyl ester, DB-370636, CS-0038574, ST50336374, Q27287338
Methyl 2-(4-nitrophenyl)acetate serves as a key intermediate in organic synthesis, particularly for pharmaceuticals and agrochemicals. It is used in peptide coupling reactions and as a building block for nitrophenyl derivatives. Researchers also employ it in material science for functionalized polymer synthesis. Its stability and reactivity make it suitable for catalytic and stoichiometric transformations.
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