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Atomfair Ethyl (3-nitrophenyl)acetate C10H11NO4
Description Ethyl (3-nitrophenyl)acetate (CAS No. 14318-64-0) is a high-purity organic ester compound with the molecular formula C10H11NO4. This nitro-substituted phenyl acetate derivative is widely utilized in synthetic organic chemistry and pharmaceutical research due to its versatile reactivity. The compound features an ethyl ester group adjacent to a 3-nitrophenyl moiety, making it a valuable intermediate for the synthesis of fine chemicals, agrochemicals, and active pharmaceutical ingredients (APIs). Our product is rigorously tested to ensure >98% purity (HPLC/GC) and is supplied in sealed, light-resistant packaging to maintain stability. Ideal for nucleophilic substitution reactions, hydrogenation, or as a precursor for heterocyclic synthesis, this…
Description
Description
Ethyl (3-nitrophenyl)acetate (CAS No. 14318-64-0) is a high-purity organic ester compound with the molecular formula C10H11NO4. This nitro-substituted phenyl acetate derivative is widely utilized in synthetic organic chemistry and pharmaceutical research due to its versatile reactivity. The compound features an ethyl ester group adjacent to a 3-nitrophenyl moiety, making it a valuable intermediate for the synthesis of fine chemicals, agrochemicals, and active pharmaceutical ingredients (APIs).
Our product is rigorously tested to ensure >98% purity (HPLC/GC) and is supplied in sealed, light-resistant packaging to maintain stability. Ideal for nucleophilic substitution reactions, hydrogenation, or as a precursor for heterocyclic synthesis, this reagent is a must-have for research laboratories focused on medicinal chemistry and material science applications.
- CAS No: 14318-64-0
- Molecular Formula: C10H11NO4
- Molecular Weight: 209.20
- Exact Mass: 209.06880783
- Monoisotopic Mass: 209.06880783
- IUPAC Name: ethyl 2-(3-nitrophenyl)acetate
- SMILES: CCOC(=O)CC1=CC(=CC=C1)[N+](=O)[O-]
- Synonyms: 14318-64-0, Ethyl (3-nitrophenyl)acetate, DTXSID60566713, DTXCID60517487, ethyl 2-(3-nitrophenyl)acetate
Application
Ethyl (3-nitrophenyl)acetate serves as a key building block in organic synthesis, particularly for constructing complex nitroaromatic compounds. Researchers employ this ester in pharmaceutical development for creating potential drug candidates with nitroaryl pharmacophores. The compound’s reactivity makes it valuable for studying structure-activity relationships in medicinal chemistry programs. It also finds use in materials science as a precursor for specialty polymers and dyes.
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