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Atomfair Methyl 2-nitro-4-(trifluoromethyl)benzoate C9H6F3NO4

Description Methyl 2-nitro-4-(trifluoromethyl)benzoate (CAS No. 228418-45-9) is a high-purity organic compound with the molecular formula C9H6F3NO4. This aromatic ester features a nitro group and a trifluoromethyl group on the benzene ring, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. Its precise structure, methyl 2-nitro-4-(trifluoromethyl)benzoate , ensures consistent reactivity for nucleophilic substitution, reduction, and cross-coupling reactions. Available in >98% purity (HPLC), this compound is supplied in rigorously tested batches with detailed analytical certificates (COA). Ideal for lab-scale and process chemistry applications, it is packaged under inert conditions to ensure stability and longevity.

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Description

Description

Methyl 2-nitro-4-(trifluoromethyl)benzoate (CAS No. 228418-45-9) is a high-purity organic compound with the molecular formula C9H6F3NO4. This aromatic ester features a nitro group and a trifluoromethyl group on the benzene ring, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. Its precise structure, methyl 2-nitro-4-(trifluoromethyl)benzoate, ensures consistent reactivity for nucleophilic substitution, reduction, and cross-coupling reactions. Available in >98% purity (HPLC), this compound is supplied in rigorously tested batches with detailed analytical certificates (COA). Ideal for lab-scale and process chemistry applications, it is packaged under inert conditions to ensure stability and longevity.

  • CAS No: 228418-45-9
  • Molecular Formula: C9H6F3NO4
  • Molecular Weight: 249.14
  • Exact Mass: 249.02489216
  • Monoisotopic Mass: 249.02489216
  • IUPAC Name: methyl 2-nitro-4-(trifluoromethyl)benzoate
  • SMILES: COC(=O)C1=C(C=C(C=C1)C(F)(F)F)[N+](=O)[O-]
  • Synonyms: Methyl 2-nitro-4-(trifluoromethyl)benzoate, 228418-45-9, DTXSID70460955, DTXCID60411774, MFCD08282772

Application

Methyl 2-nitro-4-(trifluoromethyl)benzoate serves as a key building block in the synthesis of agrochemicals, pharmaceuticals, and specialty materials. Its nitro and trifluoromethyl groups enable facile functionalization for creating bioactive molecules or fluorinated polymers. Researchers utilize it in palladium-catalyzed cross-coupling reactions to construct complex aromatic systems. The compound is also employed in the development of radiotracers and positron emission tomography (PET) ligands due to its fluorine-rich structure.

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