CAS 2593-31-9
:N-hydroxy-4-iodobenzamide
Description:
N-hydroxy-4-iodobenzamide is an organic compound characterized by the presence of a hydroxylamine functional group (-NHOH) attached to a benzamide structure, specifically at the para position relative to the amide group. This compound features an iodine atom substituted at the 4-position of the benzene ring, which can influence its reactivity and biological activity. N-hydroxy-4-iodobenzamide is typically a white to off-white solid and is soluble in polar organic solvents. The presence of both the hydroxylamine and the iodine substituent can impart unique properties, such as potential reactivity in nucleophilic substitution reactions and the ability to participate in various chemical transformations. This compound may also exhibit biological activity, making it of interest in medicinal chemistry and drug development. Safety data should be consulted for handling, as compounds with iodine can pose health risks. Overall, N-hydroxy-4-iodobenzamide is a versatile compound with applications in research and potential therapeutic uses.
Formula:C7H6INO2
Synonyms:- 4-iodo-N-hydroxybenzamide
- N-hydroxy-4-iodobenzamide
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Found 5 products.
4-Iodo-N-hydroxybenzamide
CAS:Formula:C7H6INO2Purity:98%Color and Shape:SolidMolecular weight:263.0325N-Hydroxy-4-iodobenzamide
CAS:<p>N-Hydroxy-4-iodobenzamide is a hydroxamic acid that is used in organic synthesis for the formation of alkenylations, carboxylates and amides. It reacts with formamide to yield formyl groups. The activated hydroxamic acid undergoes reductive elimination to produce an amine group. N-Hydroxy-4-iodobenzamide has been shown to react with biomolecules such as proteins and nucleic acids. Mechanistic studies have shown that this reaction proceeds through a formyl intermediate, which can be reduced by formaldehyde or sodium borohydride.</p>Formula:C7H6INO2Purity:Min. 95%Molecular weight:263.03 g/mol
