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

Uses

3,5-Diiodoanaline is used as a reactant in the preparation of triiodobenzene for the synthesis of phenylacetlene-based conjugated dendrimers with unsymmetrical branching.

Upstream product

• 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 
• 53663-23-3 1,2,3-triiodo-5-nitrobenzene 
• 57830-60-1 3,5-diiodonitrobenzene 

Downstream Products

• 57598-13-7 3,5-diiodobenzenesulfonyl chloride 
• 1454620-38-2 2-[6-anilino-1,3,5-hexatrienyl]-4,6-diiodo-1,3,3-trimethyl-3H-indolium iodide 
• 1454620-41-7 (3,5-diiodophenyl)hydrazine 
• 1570074-99-5 C₁₄H₁₆I₂N₂O₄ 
• 1395491-80-1 C₃₀H₂₅N₃O₂ 
• 402956-36-9 3,5-diethynylaniline 
• 1248386-96-0 3,5-bis(pyridine-4-ylethynyl)aniline 
• 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