
CAS 709-73-9
:N-(3,5-Difluoro-4-iodophenyl)acetamide
Description:
N-(3,5-Difluoro-4-iodophenyl)acetamide, with the CAS number 709-73-9, is an organic compound characterized by its acetamide functional group attached to a phenyl ring that is substituted with both fluorine and iodine atoms. The presence of the difluoro and iodo substituents on the aromatic ring significantly influences its chemical properties, including its reactivity and polarity. This compound typically exhibits a solid state at room temperature and is soluble in organic solvents, reflecting its non-polar characteristics due to the halogen substitutions. The difluoro groups can enhance the compound's lipophilicity, while the iodine atom may contribute to its potential biological activity. N-(3,5-Difluoro-4-iodophenyl)acetamide is of interest in medicinal chemistry and materials science, where it may serve as a precursor or intermediate in the synthesis of more complex molecules. Its unique combination of halogen atoms can also affect its electronic properties, making it a subject of study in various chemical applications.
Formula:C8H6F2INO
InChI:InChI=1S/C8H6F2INO/c1-4(13)12-5-2-6(9)8(11)7(10)3-5/h2-3H,1H3,(H,12,13)
InChI key:InChIKey=BNHPMNGLQXKZHB-UHFFFAOYSA-N
SMILES:N(C(C)=O)C1=CC(F)=C(I)C(F)=C1
Synonyms:- Acetanilide, 3′,5′-difluoro-4′-iodo-
- Acetamide, N-(3,5-difluoro-4-iodophenyl)-
- N-(3,5-Difluoro-4-iodophenyl)acetamide
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