90064-46-3

Usage

Uses

Used in Pharmaceutical Industry:
1-CHLORO-4-IODO-2,5-DIMETHOXYBENZENE is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the formation of complex molecular structures that can exhibit therapeutic properties.
Used in Organic Materials Synthesis:
1-CHLORO-4-IODO-2,5-DIMETHOXYBENZENE serves as a building block for various heterocyclic compounds, which are essential in the development of organic materials with specific properties and applications.
Used in Chemical Research:
1-CHLORO-4-IODO-2,5-DIMETHOXYBENZENE is utilized in chemical research to explore its reactivity and potential applications in the synthesis of new compounds and materials, further expanding its utility in various industries.

InChI:InChI=1/C8H8ClIO2/c1-11-7-4-6(10)8(12-2)3-5(7)9/h3-4H,1-2H3

Upstream product

• 2100-42-7 2-chloro-1,4-dimethoxybenzene 
• 6940-53-0 4-chloro-2,5-dimethoxy nitrobenzene 
• 615-67-8 chloro-p-hydroquinone 
• 150-78-7 1,4-dimethoxybezene 
• 6358-64-1 4-chloro-2,5-dimethoxy-aniline 
• 25245-35-6 1-iodo-2,4-dimethoxybenzene 

Downstream Products

• 90064-48-5 4-chloro-2,5-dimethoxybenzaldehyde 
• 7310-97-6 2,5-dimethoxyterephthalaldehyde 
• 203579-49-1 2-chloro-5-iodo-1,4-benzoquinone 
• 1280218-05-4 C₉H₈ClF₃O₂ 

Relevant academic research and scientific papers

A facile synthesis of 1,4-dialkoxy-2,5-diiodobenzenes: reaction of dialkoxybenzenes with iodine monochloride in alcoholic solvents

A facile synthesis of 1,4-dialkoxy-2,5-diiodobenzenes via diiodination of the corresponding dialkoxybenzenes with iodine monochloride has been developed. Employment of ah alcoholic solvent as a reaction medium is crucial for attaining a high yield; the reaction in a nonalcoholic solvent usually resulted in a poor yield. The diiodobenzene derivatives are useful intermediates in the synthesis of such advanced materiais as soluble phenylenevinylene polymers anal dialkoxy derivatives of 7,7,8,8-tetracyanoquinodimethane.

Multistep Reversible Redox Systems, LXIII. 2,5-Disubstituted N,N'-Dicyanoquinone Diimines (DCNQIs) - Syntheses, and Redox Properties

Quinones 1a-q and DCNQIs 2a-g have been synthesized in order to investigate substituent effects.It was necessary to employ novel synthetic routes for the introduction of iodine into 1f (7), the trifluoromethyl group into 1g-i, deuterium into 1m-p, and esp

Radiohalogen-Labeled Imaging Agents. 3. Compounds for Measurement of Brain Blood Flow by Emission Tomography

The radioiodine-labeled amines currently available as brain-imaging agents, based on our previous work and that of others, are prepared either by exchange labeling or by direct iodination of a protected intermediate.The intrinsic slowness of these process