20981-79-7

Usage

Uses

Used in Organic Synthesis:
3,5-diiodophenol is used as a reagent in organic synthesis for the preparation of various pharmaceuticals and dyes. Its iodine atoms facilitate specific chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
3,5-diiodophenol is used as a precursor to other iodinated compounds, which are essential in the development of pharmaceuticals. Its presence in these compounds can enhance their therapeutic properties, such as antiseptic or anti-inflammatory effects.
Used in Dye Production:
3,5-diiodophenol is used as a building block in the production of specialty dyes. Its unique chemical structure allows for the creation of dyes with specific color characteristics and properties, suitable for various applications.
Used in Radiopharmaceuticals and Medical Imaging:
Due to its strong iodine content, 3,5-diiodophenol has potential applications in radiopharmaceuticals and medical imaging. It can be used to create contrast agents for imaging studies, aiding in the diagnosis of various medical conditions.
Safety Precautions:
It is important to handle 3,5-diiodophenol with caution, as iodine-containing chemicals can be toxic. Proper handling should include working in a well-ventilated environment and using appropriate personal protective equipment to minimize exposure risks.

Upstream product

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• 5327-44-6 3,5-dinitroanisole 
• 116529-49-8 2,4-diiodo-6-nitroaniline 
• 57830-60-1 3,5-diiodonitrobenzene 
• 626-44-8 1,3,5-Triiodobenzene 

Downstream Products

• 89465-93-0 2,3,4,5-tetraiodo-phenol 
• 101654-26-6 (3,5-diiodo-phenoxy)-acetic acid 
• 608527-84-0 6-(3,5-diiodophenoxy)hexan-1-ol 
• 263706-96-3 3,5-bis-[2-(2,5-dipropyloxy-4-{2-[3-(tetrahydro-2H-pyran-2-yloxy)-5-ethynylphenyl]ethynyl}phenyl)ethynyl]toluene 
• 350589-39-8 3,5-bis-[2-(2,5-dipropyloxy-4-{2-[5-iod-3-(tetrahydro-2H-pyran-2-yloxy)phenyl]ethynyl}phenyl)ethynyl]toluene 
• 350589-43-4 3,5-bis-[2-(2,5-dipropyloxy-4-{2-[3-(tetrahydro-2H-pyran-2-yloxy)-5-(2-trimethylsilylethynyl)phenyl]ethynyl}phenyl)ethynyl]toluene 
• 1044811-13-3 1-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)-3,5-diiodobenzene 
• 1037290-36-0 C₄₆H₈₄I₂O₁₉ 
• 598297-31-5 trifluoro-methanesulfonic acid 3,5-bis-[4,5-bis-(3,5-di-tert-butyl-phenylethynyl)-2-methoxy-phenylethynyl]-phenyl ester 
• 918826-08-1 3,5-diethynyl-phenol 
• 608527-85-1 6-[3,5-bis{2-(4-{2-[3-tert-butyl-5-(2-triisopropylsilylethynyl)]phenylethynyl}phenylethynyl)}phenoxy]hexyl benzoate 
• 608527-86-2 6-[3,5-bis(2-{4-[2-(3-tert-butyl-5-ethynyl)phenylethynyl]phenylethynyl})phenoxy]hexyl benzoate 
• 608527-83-9 6-(3,5-diiodophenoxy)hexyl benzoate 
• 882508-13-6 5-(3,5-Diiodo-phenoxymethyl)-1,2,3-tris-hexadecyloxy-benzene 

Relevant academic research and scientific papers

A Pronounced Halogen Effect on the Organogelation Properties of Peripherally Halogen Functionalized Poly(benzyl ether) Dendrons

An interesting halogen-substituent effect on the organogelation properties of poly(benzyl ether) dendrons is reported. A new class of poly(benzyl ether) dendrons with halo substituents decorating their periphery was synthesized and fully characterized. A

Molecular Tectonics. Porous Hydrogen-Bonded Networks Built from Derivatives of Pentaerythrityl Tetraphenyl Ether

The symmetric four-armed geometry of pentaerythrityl tetraphenyl ether (5) makes it a valuable starting point for building complex molecular and supramolecular structures. In particular, it provides a core to which multiple sites of attractive intermolecular interaction can be attached, thereby creating compounds predisposed to form complex networks by association. To facilitate exploitation of the pentaerythrityl tetraphenyl ether core in such ways, we have prepared more than 20 new derivatives by efficient methods. Of special interest are compounds 3 and 4, which incorporate four diaminotriazine groups attached to the meta and para positions of the pentaerythrityl tetraphenyl ether core. Crystallization of compounds 3 and 4 from DMSO/dioxane is directed by hydrogen bonding of the diaminotriazine groups according to well-established motifs, thereby producing three-dimensional networks. In forming these networks, each molecule of compound 3 forms a total of 12 hydrogen bonds with six others, whereas each molecule of compound 4 forms a total of 16 hydrogen bonds with four others. Both networks are highly porous and define significant interconnected channels for the inclusion of guests. In crystals of compounds 3 and 4, the fraction of the volume accessible to guests is 66% and 57%, respectively. In both cases, the pentaerythrityl tetraphenyl ether cores adopt conformations that deviate substantially from tetrahedral geometry. It is noteworthy that the inherent flexibility of the core does not favor the formation of close-packed guest-free structures.

Synthesis, aggregation, and adsorption phenomena of shape-persistent macrocycles with extraannular polyalkyl substituents

The synthesis of shape-persistent macrocycles based on the phenyl-ethynyl backbone containing various extraannular alkyl side chains is described. Although compound solubility increases with increasing size of the side groups, decreasing the solvent polar