915706-87-5

Usage

Structure

Derivative of benzene with two iodine atoms and two hydroxymethyl groups attached to the benzene ring

Application

Commonly used in organic synthesis
Building block in the production of pharmaceuticals and agrochemicals
Employed in the synthesis of dyes
Serves as a reagent in organic chemical reactions

Versatility

Exhibits a wide range of applications in the field of chemistry.

Upstream product

• 589-29-7 p-xylylene glycol 
• 915706-86-4 2,5-diiodo-1,4-bis(hydroxymethyl)benzene diacetate 
• 14720-70-8 1,4-bis(hydroxymethyl)benzene diacetate 

Downstream Products

• 56403-29-3 2,5-diiodo-1,4-bis(bromomethyl)benzene 
• 1231999-67-9 2,5-diiodo-1,4-benzenedicarboxaldehyde 
• 371953-92-3 (2,5-bis(phenylethynyl)-1,4-phenylene)dimethanol 
• 882880-02-6 4-hydroxymethyl-2,5-bis(trimethylsilylethynyl)benzyl alcohol 
• 20856-80-8 2,5-diiodo-1,4-dibenzoic acid 
• 1235713-11-7 C₇₀H₁₀₆O₆Si₂ 
• 13064-64-7 2,5-diiodo-1,4-hydroquinone 

Relevant academic research and scientific papers

Synthesis and Physicochemical Properties of Dibenzo[2,3- d:2′,3′- d′]anthra[1,2- b:5,6- b′]dithiophene (DBADT) and Its Derivatives: Effect of Substituents on Their Molecular Orientation and Transistor Properties

We have synthesized dibenzo[2,3-d:2′,3′-d′]anthra[1,2-b:5,6-b′]dithiophene (DBADT) and several derivatives bearing alkyl and phenyl groups at various positions. The optical and electrochemical properties of the synthesized compounds were investigated. All

Step-Growth Copolymerization Between an Immobilized Monomer and a Mobile Monomer in Metal–Organic Frameworks

The A–A/B–B step-growth copolymerization between a monomer immobilized in the crystalline state and a monomer mobile in the solution state is demonstrated. One of the two monomers was immobilized as organic ligands of the metal–organic framework (MOF) and

A practical synthesis of 1,4-diiodo-2,5-bis(chloromethyl)benzene and 1,4-diiodo-2,5-bis(bromomethyl)benzene

Iodination of protected bis(hydroxymethyl)benzene, deprotection of the resulting diiodo aromatics, and subsequent transformation of the hydroxymethyl groups to benzyl halides provides an easy and reliable way to the pure title compounds. Georg Thieme Verl

Photophysics, aggregation and amplified quenching of a water-soluble poly(phenylene ethynylene).

The fluorescence, absorption and fluorescence quenching properties of an anionic poly(phenylene ethynylene) are investigated in H2O and MeOH solutions.