Description

Ethyl 2-(2,4-dichlorophenyl)acetate (CAS No. 41022-54-2) is a high-purity organic ester compound with the molecular formula C₁₀H₁₀Cl₂O₂. This specialized chemical is widely used in pharmaceutical and agrochemical research due to its role as a key intermediate in synthetic pathways. The compound features a dichlorophenyl moiety esterified with ethyl acetate, offering unique reactivity for nucleophilic substitutions and coupling reactions. Our product is synthesized under strict quality control, ensuring >98% purity by HPLC analysis, and is supplied in amber glass vials under inert atmosphere to prevent degradation. Ideal for medicinal chemistry applications, this reagent is particularly valuable in the development of chlorinated aromatic compounds with potential biological activity. Technical specifications include molecular weight of 233.09 g/mol, boiling point of 285-287°C, and density of 1.28 g/cm³. Available in research quantities from 100mg to 1kg scale, with custom synthesis options available for bulk requirements.

Properties

• CAS Number: 41022-54-2
• Complexity: 197
• IUPAC Name: ethyl 2-(2,4-dichlorophenyl)acetate
• InChI: InChI=1S/C10H10Cl2O2/c1-2-14-10(13)5-7-3-4-8(11)6-9(7)12/h3-4,6H,2,5H2,1H3
• InChI Key: GQKNWRRUKBQMFY-UHFFFAOYSA-N
• Exact Mass: 232.0057849
• Molecular Formula: C10H10Cl2O2
• Molecular Weight: 233.09
• SMILES: CCOC(=O)CC1=C(C=C(C=C1)Cl)Cl
• Topological: 26.3
• Monoisotopic Mass: 232.0057849
• Synonyms: 41022-54-2, ethyl 2-(2,4-dichlorophenyl)acetate, Ethyl 2,4-dichlorophenylacetate, MFCD01566538, ethyl (2,4-dichlorophenyl)acetate, NSC33951, SCHEMBL707398, DTXSID70961391, ethyl 2,4-dichloro-benzeneacetate, GQKNWRRUKBQMFY-UHFFFAOYSA-N, ethyl2-(2,4-dichlorophenyl)acetate, NSC-33951, SBB098049, AKOS005254596, AS-11981, CS-0199422, D93426

This compound serves as a versatile building block in organic synthesis, particularly for creating chlorinated aromatic pharmaceuticals. Researchers utilize it in developing potential fungicides and herbicides due to its dichlorophenyl structure. The ester functionality allows for further transformations including hydrolysis to acids or reduction to alcohols. In medicinal chemistry, it’s employed as a precursor for non-steroidal anti-inflammatory drug (NSAID) analogs. The compound also finds use in material science for synthesizing specialty polymers with enhanced stability.

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