CAS 7212-28-4

Acetamide, 2-iodo-N-phenyl-

Description:

Acetamide, 2-iodo-N-phenyl- is an organic compound characterized by the presence of an acetamide functional group and a phenyl ring, with an iodine atom substituted at the second position of the acetamide. Its molecular formula typically includes carbon, hydrogen, nitrogen, and iodine, reflecting its structure. This compound is often used in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals and agrochemicals. The presence of the iodine atom can impart unique reactivity, making it useful in nucleophilic substitution reactions. Additionally, the phenyl group contributes to the compound's hydrophobic characteristics, influencing its solubility and interaction with biological systems. Acetamide derivatives, including this compound, may exhibit specific biological activities, which can be explored in medicinal chemistry. Safety data should be consulted, as halogenated compounds can pose health risks, and appropriate handling procedures should be followed in laboratory settings. Overall, 2-iodo-N-phenyl-acetamide is a valuable compound in synthetic organic chemistry with potential applications in various fields.

Formula: C₈H₈INO

Synonyms:

• 2-iodo-N-phenylacetamide
• Acetamide, 2-iodo-N-phenyl-

Acetamide, 2-iodo-N-phenyl-

CAS: 7212-28-4

Formula: C₈H₈INO

Purity: 95%

Color and Shape: Solid

Molecular weight: 261.0597

Ref: IN-DA00IMN6

2-Iodo-N-Phenylacetamide

CAS: 7212-28-4

2-Iodo-N-Phenylacetamide

Purity: 95%

Molecular weight: 261.06g/mol

Ref: 54-OR1025803

2-Iodo-N-phenylacetamide

CAS: 7212-28-4

Formula: C₈H₈INO

Purity: 95%

Color and Shape: Liquid, No data available.

Molecular weight: 261.062

Ref: 10-F234369

2-Iodo-N-phenylacetamide

CAS: 7212-28-4

2-Iodo-N-phenylacetamide (2IA) is a chemical that binds to the substrate binding site of the enzyme. It has been shown to have pro-inflammatory cytokine activity in vitro and in vivo. 2IA is a member of a class of compounds that are able to inhibit chronic viral infections by inhibiting the production of pro-inflammatory cytokines. The chemical diversity of 2IA is due to its functional groups, which include an electrospray ionization quadrupole, a phosphate group, and a disulfide bond. 2IA also has been shown to inhibit phosphorylation reactions in biochemical pathways.

Formula: C₈H₈INO

Purity: Min. 95%

Molecular weight: 261.06 g/mol

Ref: 3D-HAA21228