1998-58-9

Usage

Uses

Used in Organic Synthesis:
2,3,5,6-Tetrafluoro-4-iodophenol is used as a building block in organic synthesis for the production of a variety of chemical compounds. Its unique structure allows for versatile reactions and modifications, contributing to the creation of new and diverse organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,3,5,6-Tetrafluoro-4-iodophenol serves as an important intermediate in the development of new drugs and pharmaceuticals. Its potential applications in medicinal chemistry are vast, as the presence of fluorine and iodine atoms can significantly influence the pharmacokinetics, pharmacodynamics, and overall efficacy of the resulting compounds.
Used in Medicinal Chemistry Development:
2,3,5,6-Tetrafluoro-4-iodophenol is utilized in the field of medicinal chemistry for the design and synthesis of novel drug candidates. The presence of fluorine and iodine atoms on the phenolic ring can enhance the lipophilicity, metabolic stability, and target binding affinity of the resulting drug molecules, thereby improving their therapeutic potential.

InChI:InChI=1/C6HF4IO/c7-1-3(9)6(12)4(10)2(8)5(1)11/h12H

Upstream product

• 827-15-6 1,2,3,4,5-pentafluoro-6-iodobenzene 

Downstream Products

• 1099822-89-5 C₆HF₄IO*C₁₄H₁₃NO 
• 1253825-26-1 4-(4-decyloxyphenyl)-2,3,5,6-tetrafluoroiodobenzoate 
• 160427-63-4 4-(4-hexoxyphenyl)-2,3,5,6-tetrafluoroiodobenzoate 
• 1253825-34-1 4'-(4-hexyloxy-2,3,5,6-tetrafluorobenzoyloxy)-2',3',5',6'-tetrafluoroiodobenzene 
• 1253825-39-6 4'-(4-decyloxy-2,3,5,6-tetrafluorobenzoyloxy)-2',3',5',6'-tetrafluoroiodobenzene 
• 1744-45-2 1,2,4,5-tetrafluorobenzene-3-iodo-6-methoxybenzene 
• 1613535-12-8 4-(pyrrolidino)pyridinium iodotetrafluorophenate 
• 1613535-11-7 4-(N,N-dimethylamino)pyridinium iodotetrafluorophenate 
• 1613535-10-6 morpholinium iodotetrafluorophenate 

Relevant academic research and scientific papers

Competing hydrogen-bond and halogen-bond donors in crystal engineering

In order to study the structure-directing competition between hydrogen- and halogen-bond donors we have synthesized two ligands, 3,3′-azobipyridine and 4,4′-azobipyridine, and co-crystallized them with a series of bi-functional donor molecules comprising

Thermoresponsive luminescence properties of polyfluorinated bistolane-type light-emitting liquid crystals

We developed and characterized four polyfluorinated bistolane derivatives. These compounds, which possess either two alkoxy substituents or an alkoxy group and a bromine atom in their two molecular terminals, were synthesized from readily available 4-alko

Structure-function relationships in liquid-crystalline halogen-bonded complexes

New liquid-crystalline materials were prepared by self-assembly driven by halogen bonding between a range of 4-alkoxystilbazoles, 4-alkyl-, and 4-alkoxy-substituted pyridines as halogen-bonding acceptors, and substituted derivatives of4-iodotetrafluorophenyl as halogen-bonding donors. Despite the fact that the starting materials are not mesomorphic, the dimeric, halogen-bonded complexes obtained exhibited nemetic and SmA phases, depending on the length of the alkylchains present on the components. The modularity of this approach also led to new chiral mesogens starting from non-mesomorphic chiral compounds.