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Atomfair 5-Chloro-2-methyl-6-nitro-1,3-benzoxazole C8H5ClN2O3

Description 5-Chloro-2-methyl-6-nitro-1,3-benzoxazole (CAS No. 13452-16-9) is a high-purity heterocyclic organic compound with the molecular formula C8H5ClN2O3. This benzoxazole derivative is characterized by its chloro, methyl, and nitro functional groups, making it a versatile intermediate for pharmaceutical, agrochemical, and materials science research. Our product is rigorously tested to ensure ??98% purity (HPLC/GC), with detailed analytical reports (COA) available upon request. Suitable for use in organic synthesis, cross-coupling reactions, and as a building block for bioactive molecules. Packaged under inert gas in amber glass vials to ensure stability and longevity.

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Description

Description

5-Chloro-2-methyl-6-nitro-1,3-benzoxazole (CAS No. 13452-16-9) is a high-purity heterocyclic organic compound with the molecular formula C8H5ClN2O3. This benzoxazole derivative is characterized by its chloro, methyl, and nitro functional groups, making it a versatile intermediate for pharmaceutical, agrochemical, and materials science research. Our product is rigorously tested to ensure ??98% purity (HPLC/GC), with detailed analytical reports (COA) available upon request. Suitable for use in organic synthesis, cross-coupling reactions, and as a building block for bioactive molecules. Packaged under inert gas in amber glass vials to ensure stability and longevity.

  • CAS No: 13452-16-9
  • Molecular Formula: C8H5ClN2O3
  • Molecular Weight: 212.59
  • Exact Mass: 211.9988697
  • Monoisotopic Mass: 211.9988697
  • IUPAC Name: 5-chloro-2-methyl-6-nitro-1,3-benzoxazole
  • SMILES: CC1=NC2=CC(=C(C=C2O1)[N+](=O)[O-])Cl
  • Synonyms: 5-chloro-2-methyl-6-nitro-1,3-benzoxazole, 13452-16-9, DTXSID30377454, DTXCID90328482, 5-chloro-2-methyl-6-nitrobenzoxazole

Application

5-Chloro-2-methyl-6-nitro-1,3-benzoxazole serves as a key intermediate in the synthesis of pharmaceuticals, particularly for developing antimicrobial and antitumor agents. Its nitro and chloro substituents enable participation in nucleophilic aromatic substitution (SNAr) and metal-catalyzed coupling reactions. Researchers also utilize this compound in the design of fluorescent probes and agrochemicals due to its benzoxazole core. Ideal for exploring structure-activity relationships (SAR) in medicinal chemistry.

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