CAS 19230-45-6
:N-(3-Iodophenyl)acetamide
Description:
N-(3-Iodophenyl)acetamide is an organic compound characterized by its amide functional group, which is derived from acetic acid and an aromatic ring substituted with iodine. The molecular structure features a phenyl ring with an iodine atom positioned at the meta position relative to the acetamide group. This substitution can influence the compound's reactivity and physical properties, such as solubility and boiling point. Typically, compounds like N-(3-Iodophenyl)acetamide exhibit moderate to high polarity due to the presence of the amide group, which can engage in hydrogen bonding. The iodine atom contributes to the compound's unique electronic properties, potentially affecting its behavior in chemical reactions and interactions with biological systems. This compound may be of interest in various fields, including medicinal chemistry and materials science, due to its potential applications in drug development and as a building block for synthesizing more complex molecules. Safety and handling precautions should be observed, as with any chemical substance, particularly those containing halogens.
Formula:C8H8INO
InChI:InChI=1S/C8H8INO/c1-6(11)10-8-4-2-3-7(9)5-8/h2-5H,1H3,(H,10,11)
InChI key:InChIKey=AMUUVYMMGLMBIW-UHFFFAOYSA-N
SMILES:N(C(C)=O)C1=CC(I)=CC=C1
Synonyms:- 3-Acetamidophenyl iodide
- Acetamide, N-(3-iodophenyl)-
- Acetanilide, 3′-iodo-
- N-(3-iodophenyl)acetamide
- N-Acetyl-3-iodoaniline
- 3′-Iodoacetanilide
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Found 2 products.
N-(3-Iodophenyl)acetamide
CAS:N-(3-Iodophenyl)acetamide is a chemical compound that is used in organic synthesis. It is soluble in water and has a melting point of 154°C. N-(3-Iodophenyl)acetamide can be synthesized by reacting 3-iodoaniline with acetic anhydride. The yield of this reaction is typically high, with a product purity of over 99%. This compound is used as an energy source when it undergoes photolysis, which results in the formation of CO2 and I2. N-(3-Iodophenyl)acetamide can also be synthesized through the aliphatic amine synthesis process by reacting ethylamine with acetaldehyde. This reaction produces a yellow liquid that can be purified by adding water to it and then boiling off the excess water. The resulting liquid should be cooled before use and stored under nitrogen gas for long periods of time.Formula:C8H8INOPurity:Min. 95%Molecular weight:261.06 g/mol

