CAS 335349-57-0

5-chloro-4-iodo-2-nitrobenzenamine

Description:

5-Chloro-4-iodo-2-nitrobenzenamine is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with a chlorine atom, an iodine atom, and a nitro group, along with an amino group. The presence of these substituents influences its chemical reactivity and physical properties. The chlorine and iodine atoms are halogens, which can impart unique reactivity patterns, while the nitro group is known for its electron-withdrawing properties, affecting the compound's overall electron density. The amino group (-NH2) contributes basicity and can participate in hydrogen bonding, enhancing solubility in polar solvents. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure suggests potential applications in synthesis and as an intermediate in the production of more complex molecules. Safety data should be consulted, as halogenated compounds can pose health risks, and appropriate handling procedures should be followed in laboratory settings.

Formula: C₆H₄ClIN₂O₂

Synonyms:

• 5-Chloro-4-iodo-2-nitroaniline
• 4-Chloro-5-iodobenzene-1,2-diamine

5-Chloro-4-iodo-2-nitroaniline

CAS: 335349-57-0

Formula: C₆H₄ClIN₂O₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 298.4656

Ref: IN-DA00CKUU

5-Chloro-4-iodo-2-nitroaniline

CAS: 335349-57-0

5-Chloro-4-iodo-2-nitroaniline

Purity: 95%

Color and Shape: Solid

Molecular weight: 298.47g/mol

Ref: 54-OR72141

5-Chloro-4-iodo-2-nitroaniline

CAS: 335349-57-0

Formula: C₆H₄ClIN₂O₂

Purity: 96%

Molecular weight: 298.46

Ref: 10-F228854

5-Chloro-4-iodo-2-nitroaniline

CAS: 335349-57-0

5-Chloro-4-iodo-2-nitroaniline is a heterocycle with a cyano group. It binds to metabotropic glutamate receptors, which are ion channels that allow for the passage of ions in response to changes in the electrical potential across the membrane. 5-Chloro-4-iodo-2-nitroaniline has been shown to be an agonist of these receptors and can potentiate excitatory postsynaptic potentials at low nanomolar concentrations. This drug also has affinity for noncompetitive metabotropic glutamate receptors, which are found in the dentate gyrus region of the hippocampus and are involved in regulating excitability levels.

Formula: C₆H₄ClIN₂O₂

Purity: Min. 95%

Molecular weight: 298.47 g/mol

Ref: 3D-KNA34957