35122-96-4

Basic information

• Product Name: 3,5-DIIODOANILINE
• Synonyms: 3,5-DIIODOANILINE;3,5-DIIODOBENZENAMINE
• CAS NO: 35122-96-4
• Molecular Formula: C₆H₅I₂N
• Molecular Weight: 344.92
• Mol File: 35122-96-4.mol
• Article Data: 16

Chemical Properties

• Appearance: /
• PKA: pK1:2.37(+1) (25°C)
• CAS DataBase Reference: 3,5-DIIODOANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DIIODOANILINE(35122-96-4)
• EPA Substance Registry System: 3,5-DIIODOANILINE(35122-96-4)

Safety Data

• Hazardous Substances Data: 35122-96-4(Hazardous Substances Data)

Usage

Description

3,5-Diiodoaniline is an organic compound with the molecular formula C6H5I2N. It is characterized by the presence of two iodine atoms attached to the 3rd and 5th positions of an aniline molecule. 3,5-DIIODOANILINE is known for its reactivity and is commonly used as a building block in the synthesis of various organic compounds.

Uses

Used in Chemical Synthesis:
3,5-Diiodoaniline is used as a reactant for the preparation of triiodobenzene, which is an essential intermediate in the synthesis of phenylacetylene-based conjugated dendrimers with unsymmetrical branching. These dendrimers have potential applications in various fields, such as materials science, electronics, and pharmaceuticals, due to their unique structural and electronic properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,5-diiodoaniline can be used as a starting material for the synthesis of various iodinated drugs and contrast agents. The presence of iodine atoms in the molecule enhances its reactivity and allows for the formation of new compounds with potential therapeutic applications.
Used in Research and Development:
3,5-Diiodoaniline is also utilized in research and development for the study of chemical reactions and the development of new synthetic methods. Its unique reactivity and structural features make it an interesting compound for exploring new reaction pathways and understanding the underlying mechanisms.

Upstream product

• 57830-60-1 3,5-diiodonitrobenzene 
• 53663-23-3 1,2,3-triiodo-5-nitrobenzene 
• 88-74-4 2-nitro-aniline 
• 116529-49-8 2,4-diiodo-6-nitroaniline 
• 100-01-6 4-nitro-aniline 
• 5398-27-6 2,6-diiodo-4-nitroaniline 

Downstream Products

• 6286-37-9 acetic acid-(3,5-diiodo-anilide) 
• 20981-79-7 3,5-diiodophenol 
• 717878-65-4 N,N-diethyl-3,5-diiodoaniline 
• 954105-35-2 1-(3,5-diiodophenyl)-3,3-diethyltriaz-1-ene 
• 900518-37-8 3,5-bis(phenylethynyl)aniline 
• 1280725-31-6 C₁₃H₇I₂N₃ 
• 1280725-30-5 C₁₂H₈I₂N₂ 
• 1280725-32-7 C₁₈H₂₀I₂N₂ 
• 1280725-34-9 C₁₆H₁₀N₂ 
• 1280725-35-0 C₁₇H₉N₃ 
• 1280725-36-1 C₂₂H₂₂N₂ 
• 1280725-37-2 C₁₇H₁₂N₂O 
• 1280725-33-8 C₁₃H₁₀I₂N₂O 
• 1351616-22-2 (I₂C₆H₃NC(CH₃))2C₅H₃N 

Relevant articles and documents

Halogen bonding-enhanced electrochemical halide anion sensing by redox-active ferrocene receptors

The first examples of halogen bonding redox-active ferrocene receptors and their anion electrochemical sensing properties are reported. Halogen bonding was found to significantly amplify the magnitude of the receptor's metallocene redox-couple's voltammet

3,5-diiodo benzenesulfonyl choride preparation technology

The invention discloses a 3,5-diiodo benzenesulfonyl choride preparation technology. The preparation technology comprises the following steps: taking paranitroaniline as a raw material, performing a substitution reaction to generate 2,6-diiodo-4-nitro aniline, performing diazotization and hydrolysis on 2,6-diiodo-4-nitro aniline and performing hydrolysis to generate 3,5-diodonitrobenzene, performing a reduction reaction on the 3,5-diodonitrobenzene to generate 3,5-diiodoaniline, performing diazotization and a sulfonylation reaction on the 3,5-diiodoaniline to obtain a target compound 3,5-diiodo benzenesulfonyl choride. The technology has the advantages of easily available raw materials, simple operation and post-treatment, and high yield, and is suitable for industrial production.

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