4-Bromo-3-chloro-2-nitroaniline
Names and Identifiers of 4-Bromo-3-chloro-2-nitroaniline
CAS Number |
1000573-99-8 |
|---|---|
EC Number |
824-751-6 |
MDL Number |
MFCD09878187 |
IUPAC Name |
4-bromo-3-chloro-2-nitroaniline |
InChI |
InChI=1S/C6H4BrClN2O2/c7-3-1-2-4(9)6(5(3)8)10(11)12/h1-2H,9H2 |
InChIKey |
CQFJUGCVNFUHRZ-UHFFFAOYSA-N |
Canonical SMILES |
C1=CC(=C(C(=C1N)[N+](=O)[O-])Cl)Br |
UNSPSC Code |
12352100 |
Physical and chemical properties of 4-Bromo-3-chloro-2-nitroaniline
Acidity coefficient |
-2.10±0.10(Predicted) |
|---|---|
Boiling Point |
353.8±37.0 °C(Predicted) |
Density |
1.909±0.06 g/cm3(Predicted) |
Exact Mass |
249.91400 |
LogP |
3.69730 |
Melting Point |
100 to 104°C |
Molecular Formula |
C6H4BrClN2O2 |
Molecular Weight |
251.46500 |
PSA |
71.84000 |
Storage condition |
2-8°C(protect from light) |
Safety Information of 4-Bromo-3-chloro-2-nitroaniline
Applications of 4-Bromo-3-chloro-2-nitroaniline
4-Bromo-3-chloro-2-nitroaniline finds applications in various fields:
- Pharmaceuticals: It serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals.
- Dyes: The compound can be utilized in dye manufacturing due to its chromophoric properties.
- Research: It is used in biochemical research, particularly in studies involving enzyme inhibition and protein interactions.
Interaction Studies of 4-Bromo-3-chloro-2-nitroaniline
Interaction studies involving 4-Bromo-3-chloro-2-nitroaniline focus on its binding affinity with biological macromolecules such as proteins and nucleic acids. These studies are crucial for understanding its potential therapeutic applications and mechanisms of action. Preliminary findings suggest that it may interact with specific enzymes, influencing their activity and stability.
Biological Activity of 4-Bromo-3-chloro-2-nitroaniline
The biological activity of 4-Bromo-3-chloro-2-nitroaniline has been explored in various studies. It exhibits potential antimicrobial properties and has been investigated for its effects on different bacterial strains. Additionally, compounds with similar structures often show cytotoxicity against cancer cell lines, indicating that 4-Bromo-3-chloro-2-nitroaniline may also possess anticancer activity.
Physical sample testing spectrum (NMR) of 4-Bromo-3-chloro-2-nitroaniline
