structure of 4-Bromo-2-chloro-5-fluoroiodobenzene

4-Bromo-2-chloro-5-fluoroiodobenzene

CAS No.: 1000572-73-5
M. Wt: 335.34000
M. Fa: C6H2BrClFI
InChI Key: AFEZDAWMIXHIIV-UHFFFAOYSA-N
Appearance: Solid

Names and Identifiers of 4-Bromo-2-chloro-5-fluoroiodobenzene

CAS Number

1000572-73-5

MDL Number

MFCD09878157

IUPAC Name

1-bromo-5-chloro-2-fluoro-4-iodobenzene

InChI

InChI=1S/C6H2BrClFI/c7-3-1-4(8)6(10)2-5(3)9/h1-2H

InChIKey

AFEZDAWMIXHIIV-UHFFFAOYSA-N

Canonical SMILES

C1=C(C(=CC(=C1I)Cl)Br)F

UNSPSC Code

12352100

Physical and chemical properties of 4-Bromo-2-chloro-5-fluoroiodobenzene

Exact Mass

333.80600

LogP

3.84620

Melting Point

34 to 38°C

Molecular Formula

C6H2BrClFI

Molecular Weight

335.34000

Safety Information of 4-Bromo-2-chloro-5-fluoroiodobenzene

Pictograms

Signal Word

Warning

Safety Data Sheet

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

Applications of 4-Bromo-2-chloro-5-fluoroiodobenzene

4-Bromo-2-chloro-5-fluoroiodobenzene finds applications in various domains:

  • Pharmaceuticals: It serves as an intermediate in the synthesis of biologically active compounds and pharmaceuticals.
  • Material Science: The compound can be utilized in the development of new materials, including liquid crystals and polymers that require specific electronic properties.
  • Chemical Research: As a versatile building block in organic synthesis, it allows chemists to explore new pathways and reactions involving halogenated compounds.

Interaction Studies of 4-Bromo-2-chloro-5-fluoroiodobenzene

Interaction studies involving 4-bromo-2-chloro-5-fluoroiodobenzene typically focus on its reactivity with nucleophiles or its role in catalysis. For instance:

  • Nucleophilic Substitution Studies: Research may explore how different nucleophiles interact with the compound's aromatic system, providing insights into reaction mechanisms and kinetics.
  • Catalytic Activity: The compound's potential as a catalyst or catalyst precursor in cross-coupling reactions can also be investigated to understand its efficiency and selectivity.

Biological Activity of 4-Bromo-2-chloro-5-fluoroiodobenzene

The biological activity of 4-bromo-2-chloro-5-fluoroiodobenzene has not been extensively documented in literature, but compounds with similar halogenation patterns often exhibit significant pharmacological properties. For example, halogenated compounds are frequently investigated for their potential as antimicrobial agents, anti-inflammatory drugs, and anticancer therapies due to their ability to interact with biological targets through various mechanisms.

Physical sample testing spectrum (NMR) of 4-Bromo-2-chloro-5-fluoroiodobenzene

Physical sample testing spectrum (NMR) of 4-Bromo-2-chloro-5-fluoroiodobenzene