Atomfair 4-Amino-2,3,5,6-tetrafluorobenzamide C7H4F4N2O

Description 4-Amino-2,3,5,6-tetrafluorobenzamide (CAS No. 1548-74-9) is a high-purity fluorinated benzamide derivative with the molecular formula C7H4F4N2O . This compound is characterized by its tetrafluorinated benzene ring and an amide functional group, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its unique structure offers excellent reactivity for further functionalization, particularly in the development of fluorinated bioactive molecules. Suitable for researchers and scientists, this product is rigorously tested for quality and consistency, ensuring reliable performance in advanced chemical applications. Available in various quantities to meet laboratory and industrial needs.

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Description

Description

4-Amino-2,3,5,6-tetrafluorobenzamide (CAS No. 1548-74-9) is a high-purity fluorinated benzamide derivative with the molecular formula C7H4F4N2O. This compound is characterized by its tetrafluorinated benzene ring and an amide functional group, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its unique structure offers excellent reactivity for further functionalization, particularly in the development of fluorinated bioactive molecules. Suitable for researchers and scientists, this product is rigorously tested for quality and consistency, ensuring reliable performance in advanced chemical applications. Available in various quantities to meet laboratory and industrial needs.

  • CAS No: 1548-74-9
  • Molecular Formula: C7H4F4N2O
  • Molecular Weight: 208.11
  • Exact Mass: 208.02597540
  • Monoisotopic Mass: 208.02597540
  • IUPAC Name: 4-amino-2,3,5,6-tetrafluorobenzamide
  • SMILES: C1(=C(C(=C(C(=C1F)F)N)F)F)C(=O)N
  • Synonyms: 4-Amino-2,3,5,6-tetrafluorobenzamide, 1548-74-9, 4-Aminotetrafluorobenzamide, EINECS 216-285-1, Benzamide, 4-amino-2,3,5,6-tetrafluoro-

Application

4-Amino-2,3,5,6-tetrafluorobenzamide is widely used as a key building block in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its electron-deficient aromatic ring makes it ideal for nucleophilic substitution reactions, enabling the creation of complex fluorinated compounds. Researchers also utilize this compound in the development of advanced materials, such as liquid crystals and polymers, due to its unique electronic properties. Additionally, it serves as a precursor in the preparation of dyes and imaging agents for biomedical applications.

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