structure of 2,4-Dibromo-3-chloro-6-fluoroaniline

2,4-Dibromo-3-chloro-6-fluoroaniline

CAS No.: 1000573-39-6
M. Wt: 303.35400
M. Fa: C6H3Br2ClFN
InChI Key: SBMUPMZTUMIDOP-UHFFFAOYSA-N

Names and Identifiers of 2,4-Dibromo-3-chloro-6-fluoroaniline

CAS Number

1000573-39-6

MDL Number

MFCD09878174

IUPAC Name

2,4-dibromo-3-chloro-6-fluoroaniline

InChI

InChI=1S/C6H3Br2ClFN/c7-2-1-3(10)6(11)4(8)5(2)9/h1H,11H2

InChIKey

SBMUPMZTUMIDOP-UHFFFAOYSA-N

Canonical SMILES

NC1=C(F)C=C(Br)C(Cl)=C1Br

UNSPSC Code

12352100

Physical and chemical properties of 2,4-Dibromo-3-chloro-6-fluoroaniline

Exact Mass

300.83000

LogP

4.16750

Molecular Formula

C6H3Br2ClFN

Molecular Weight

303.35400

PSA

26.02000

Safety Information of 2,4-Dibromo-3-chloro-6-fluoroaniline

Pictograms

Signal Word

 Warning

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of 2,4-Dibromo-3-chloro-6-fluoroaniline

2,4-Dibromo-3-chloro-6-fluoroaniline has several applications across various fields:

  • Pharmaceuticals: Due to its biological activity as an enzyme inhibitor, it is studied for potential use in drug development.
  • Agricultural chemicals: The compound may serve as an intermediate in the synthesis of agrochemicals or pesticides.
  • Material science: Its unique properties make it a candidate for developing novel materials with specific electronic or optical characteristics.

Interaction Studies of 2,4-Dibromo-3-chloro-6-fluoroaniline

Interaction studies involving 2,4-dibromo-3-chloro-6-fluoroaniline focus on its effects on biological systems and its interactions with other chemical compounds. For instance:

  • Studies have indicated that this compound may affect metabolic pathways involving cytochrome P450 enzymes.
  • Understanding its interactions with other drugs can provide insights into potential drug-drug interactions in therapeutic contexts.

Biological Activity of 2,4-Dibromo-3-chloro-6-fluoroaniline

Research has shown that 2,4-dibromo-3-chloro-6-fluoroaniline exhibits significant biological activity. It has been identified as an inhibitor of certain cytochrome P450 enzymes, specifically CYP1A2 and CYP2C9. This inhibition suggests potential applications in pharmacology and toxicology, particularly in understanding drug metabolism and interactions.