20981-79-7

Basic information

• Product Name: 3,5-diiodophenol
• Synonyms: 3,5-diiodophenol
• CAS NO: 20981-79-7
• Molecular Formula: C₆H₄I₂O
• Molecular Weight: 345.9043
• Mol File: 20981-79-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• PKA: pK1:8.103 (25°C)
• CAS DataBase Reference: 3,5-diiodophenol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-diiodophenol(20981-79-7)
• EPA Substance Registry System: 3,5-diiodophenol(20981-79-7)

Safety Data

• Hazardous Substances Data: 20981-79-7(Hazardous Substances Data)

Usage

General Description

3,5-diiodophenol, also known as 3,5-diiodo-1-hydroxybenzene, is a chemical compound with the molecular formula C6H4I2O. It is a derivative of phenol, featuring two iodine atoms attached to the 3 and 5 positions of the benzene ring. 3,5-diiodophenol is commonly used as a reagent in organic synthesis, particularly in the preparation of various pharmaceuticals and dyes. It is also utilized as a precursor to other iodinated compounds and as a building block in the production of specialty chemicals. Due to its strong iodine content, 3,5-diiodophenol has potential applications in radiopharmaceuticals and medical imaging. However, it is important to handle this compound with caution, as iodine-containing chemicals can be toxic and should be used in a well-ventilated environment with appropriate personal protective equipment.

Upstream product

• 5327-44-6 3,5-dinitroanisole 
• 626-44-8 1,3,5-Triiodobenzene 
• 35122-96-4 3,5-diiodoaniline 
• 344324-66-9 1,3-diiodo-5-methoxybenzene 
• 88-74-4 2-nitro-aniline 
• 116529-49-8 2,4-diiodo-6-nitroaniline 
• 57830-60-1 3,5-diiodonitrobenzene 

Downstream Products

• 90917-53-6 2-(3,5-diiodo-phenoxy)-butyric acid 
• 89465-93-0 2,3,4,5-tetraiodo-phenol 
• 101654-26-6 (3,5-diiodo-phenoxy)-acetic acid 
• 882508-13-6 5-(3,5-Diiodo-phenoxymethyl)-1,2,3-tris-hexadecyloxy-benzene 
• 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 
• 1037290-36-0 C₄₆H₈₄I₂O₁₉ 
• 1044811-13-3 1-(2-(2-(2-methoxyethoxy)ethoxy)ethoxy)-3,5-diiodobenzene 
• 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 

Relevant articles and documents

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

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