Atomfair Clofenamic acid C13H9Cl2NO2

Description Clofenamic acid (CAS No. 13365-26-9), also known as 2-(2,3-dichloroanilino)benzoic acid, is a high-purity organic compound with the molecular formula C13H9Cl2NO2. This dichlorinated aromatic carboxylic acid derivative is widely utilized in pharmaceutical and biochemical research due to its non-steroidal anti-inflammatory (NSAID) properties. Our product is rigorously tested to ensure ??98% purity by HPLC, with detailed analytical reports available upon request. Supplied as a white to off-white crystalline powder, it is packaged under inert conditions to ensure stability and longevity. Ideal for researchers investigating cyclooxygenase inhibition, prostaglandin synthesis modulation, or structure-activity relationship studies in medicinal chemistry.

Description

Clofenamic acid (CAS No. 13365-26-9), also known as 2-(2,3-dichloroanilino)benzoic acid, is a high-purity organic compound with the molecular formula C₁₃H₉Cl₂NO₂. This dichlorinated aromatic carboxylic acid derivative is widely utilized in pharmaceutical and biochemical research due to its non-steroidal anti-inflammatory (NSAID) properties. Our product is rigorously tested to ensure ??98% purity by HPLC, with detailed analytical reports available upon request. Supplied as a white to off-white crystalline powder, it is packaged under inert conditions to ensure stability and longevity. Ideal for researchers investigating cyclooxygenase inhibition, prostaglandin synthesis modulation, or structure-activity relationship studies in medicinal chemistry.

CAS No: 13365-26-9
Molecular Formula: C13H9Cl2NO2
Molecular Weight: 282.12
Exact Mass: 281.0010339
Monoisotopic Mass: 281.0010339
IUPAC Name: 2-(2,3-dichloroanilino)benzoic acid
SMILES: C1=CC=C(C(=C1)C(=O)O)NC2=C(C(=CC=C2)Cl)Cl
Synonyms: Clofenamic acid, 4295-55-0, 2-(2,3-dichloroanilino)benzoic acid, Acido clofenamico, Acide clofenamique

Application

Clofenamic acid serves as a key reference standard in NSAID research, particularly for studying COX enzyme inhibition mechanisms. It is employed in in vitro models of inflammation and pain pathways due to its prostaglandin synthesis suppression capabilities. Researchers utilize this compound in structure-activity relationship studies of fenamate-class pharmaceuticals. Its dichlorinated structure makes it valuable for metabolic stability investigations in drug development pipelines.

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