6-CHLORO-4-IODO-3-METHYLANILINE
Names and Identifiers of 6-CHLORO-4-IODO-3-METHYLANILINE
CAS Number |
1000341-54-7 |
|---|---|
IUPAC Name |
2-chloranyl-4-iodanyl-5-methyl-aniline |
Canonical SMILES |
CC1=CC(=C(C=C1I)Cl)N |
Physical and chemical properties of 6-CHLORO-4-IODO-3-METHYLANILINE
Exact Mass |
266.93100 |
|---|---|
LogP |
3.41640 |
Molecular Formula |
C7H7ClIN |
Molecular Weight |
267.49500 |
PSA |
26.02000 |
Applications of 6-CHLORO-4-IODO-3-METHYLANILINE
2-Chloro-4-iodo-5-methylaniline finds applications in various fields:
- Pharmaceuticals: It serves as a precursor for synthesizing biologically active compounds.
- Agrochemicals: Its derivatives are explored for use as herbicides or fungicides due to their biological activity.
- Dyes and Pigments: The compound is utilized in producing colorants due to its stable aromatic structure.
Interaction Studies of 6-CHLORO-4-IODO-3-METHYLANILINE
Interaction studies of 2-Chloro-4-iodo-5-methylaniline focus on its reactivity with biological targets. Investigations have shown that its derivatives can interact with enzymes or receptors, potentially leading to therapeutic effects or toxicity. Studies also assess how modifications to the halogen or methyl groups affect these interactions, providing insights into optimizing efficacy and safety.
Biological Activity of 6-CHLORO-4-IODO-3-METHYLANILINE
Research indicates that 2-Chloro-4-iodo-5-methylaniline exhibits biological activity, particularly in the context of medicinal chemistry. Its derivatives have been studied for potential antimicrobial and anticancer properties. The presence of halogens often enhances biological activity due to increased lipophilicity, which facilitates cell membrane penetration.