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Atomfair Benzoic acid, 3-ethyl- C9H10O2

Description 3-Ethylbenzoic Acid (CAS No. 2393-20-6) is a high-purity aromatic carboxylic acid derivative with the molecular formula C9H10O2. This compound, also known by its IUPAC name 3-ethylbenzoic acid , features an ethyl substituent at the meta-position of the benzoic acid ring, offering unique reactivity for organic synthesis and pharmaceutical applications. Available in crystalline form with ??98% purity (HPLC), it is ideal for use as a building block in medicinal chemistry, ligand synthesis, and material science research. Packaged under inert gas to ensure stability, this product is rigorously tested for impurities (GC/MS) and complies with ACS-grade standards. Synonyms include NSC 59887…

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Description

Description

3-Ethylbenzoic Acid (CAS No. 2393-20-6) is a high-purity aromatic carboxylic acid derivative with the molecular formula C9H10O2. This compound, also known by its IUPAC name 3-ethylbenzoic acid, features an ethyl substituent at the meta-position of the benzoic acid ring, offering unique reactivity for organic synthesis and pharmaceutical applications. Available in crystalline form with ??98% purity (HPLC), it is ideal for use as a building block in medicinal chemistry, ligand synthesis, and material science research. Packaged under inert gas to ensure stability, this product is rigorously tested for impurities (GC/MS) and complies with ACS-grade standards. Synonyms include NSC 59887 and UNII-NK9G60IQ0A.

  • CAS No: 2393-20-6
  • Molecular Formula: C9H10O2
  • Molecular Weight: 150.17
  • Exact Mass: 150.068079557
  • Monoisotopic Mass: 150.068079557
  • IUPAC Name: 3-ethylbenzoic acid
  • SMILES: CCC1=CC(=CC=C1)C(=O)O
  • Synonyms: 619-20-5, Benzoic acid, 3-ethyl-, UNII-NK9G60IQ0A, NK9G60IQ0A, NSC 59887

Application

3-Ethylbenzoic acid serves as a versatile intermediate in pharmaceutical synthesis, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and liquid crystal materials. Its meta-substituted ethyl group enhances steric control in palladium-catalyzed cross-coupling reactions. Researchers also utilize it as a precursor for metal-organic frameworks (MOFs) due to its rigid aromatic backbone. In agrochemicals, it functions as a scaffold for herbicidal compounds.

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